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1.
BMC Anesthesiol ; 21(1): 162, 2021 05 26.
Artículo en Inglés | MEDLINE | ID: mdl-34039274

RESUMEN

BACKGROUND: Nicolaides-Baraitser syndrome (NCBRS) is a rare disease caused by mutations in the SMRCA2 gene, which affects chromatin remodelling and leads to a wide range of symptoms including microcephaly, distinct facial features, recurrent seizures, and severe mental retardation. Until now, less than 100 cases have been reported. CASE PRESENTATION: A 22-month old male infant with NCBRS underwent elective cleft palate surgery. The anaesthetists were challenged by the physiological condition of the patient: narrow face, very small mouth, mild tachypnea, slight sternal retractions, physical signs of partial monosomy 9p, and plagiocephalus, midface hypoplasia, V-shaped cleft palate, enhanced muscular hypotension, dysplastic kidneys (bilateral, estimated GFR: approx. 40 ml/m2), nocturnal oxygen demand, and combined apnea. In addition, little information was available about interaction of the NCBRS displayed by the patient and anaesthesia medications. CONCLUSIONS: The cleft palate was successfully closed using the bridge flap technique. Overall, we recommend to perform a trial video assisted laryngoscopy in the setting of spontaneous breathing with deep inhalative anaesthesia before administration of muscle relaxation to detect any airway difficulties while remaining spontaneoues breathing and protective reflexes.


Asunto(s)
Anestesia General/métodos , Fisura del Paladar/cirugía , Deformidades Congénitas del Pie/cirugía , Hipotricosis/cirugía , Discapacidad Intelectual/cirugía , Anestésicos por Inhalación/administración & dosificación , Facies , Deformidades Congénitas del Pie/fisiopatología , Humanos , Hipotricosis/fisiopatología , Lactante , Discapacidad Intelectual/fisiopatología , Laringoscopía/métodos , Masculino , Enfermedades Raras , Sevoflurano/administración & dosificación
2.
Am J Med Genet A ; 185(7): 2153-2159, 2021 07.
Artículo en Inglés | MEDLINE | ID: mdl-33851505

RESUMEN

Hypotrichosis-lymphedema-telangiectasia syndrome (HLTS) is a rare condition caused by pathogenic variants in the SOX18 gene. SOX18 plays a key role in angio- and lymphangiogenesis due to its expression in venous endothelial cells from which the lymphatic system develops. It is also expressed in embryonic hair follicles, heart, and vascular smooth muscle cells. The main clinical symptoms of HLTS include sparse hair, alopecia totalis, lymphedema, most often affecting lower limbs, and telangiectatic lesions. Only 10 patients with a SOX18 pathogenic variant have been described that presented with additional features such as hydrocele, renal failure, arterial or pulmonary hypertension, aortic dilatation, and facial dysmorphism. Here, we summarize these phenotypic variations and report an additional HLTS patient, with a 14-nucleotide de novo duplication in SOX18 and congenital ileal atresia, a feature not previously associated with HLTS.


Asunto(s)
Predisposición Genética a la Enfermedad , Hipotricosis/genética , Linfangiogénesis/genética , Linfedema/genética , Factores de Transcripción SOXF/genética , Telangiectasia/genética , Adolescente , Niño , Preescolar , Células Endoteliales/metabolismo , Células Endoteliales/patología , Femenino , Duplicación de Gen/genética , Humanos , Hipotricosis/fisiopatología , Lactante , Recién Nacido , Linfedema/fisiopatología , Masculino , Telangiectasia/fisiopatología
3.
Neuropediatrics ; 52(2): 109-122, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33578439

RESUMEN

Nicolaides-Baraitser syndrome (NCBRS), caused by a mutation in the SMARCA2 gene, which goes along with intellectual disability, congenital malformations, especially of face and limbs, and often difficult-to-treat epilepsy, is surveyed focusing on epilepsy and its treatment. Patients were recruited via "Network Therapy of Rare Epilepsies (NETRE)" and an international NCBRS parent support group. Inclusion criterion is NCBRS-defining SMARCA2 mutation. Clinical findings including epilepsy classification, anticonvulsive treatment, electroencephalogram (EEG) findings, and neurodevelopmental outcome were collected with an electronic questionnaire. Inclusion of 25 NCBRS patients with epilepsy in 23 of 25. Overall, 85% of the participants (17/20) reported generalized seizures, the semiology varied widely. EEG showed generalized epileptogenic abnormalities in 53% (9/17), cranial magnetic resonance imaging (cMRI) was mainly inconspicuous. The five most frequently used anticonvulsive drugs were valproic acid (VPA [12/20]), levetiracetam (LEV [12/20]), phenobarbital (PB [8/20]), topiramate (TPM [5/20]), and carbamazepine (CBZ [5/20]). LEV (9/12), PB (6/8), TPM (4/5), and VPA (9/12) reduced the seizures' frequency in more than 50%. Temporary freedom of seizures (>6 months) was reached with LEV (4/12), PB (3/8), TPM (1/5, only combined with PB and nitrazepam [NZP]), and VPA (4/12). Seizures aggravation was observed under lamotrigine (LTG [2/4]), LEV (1/12), PB (1/8), and VPA (1/12). Ketogenic diet (KD) and vagal nerve stimulation (VNS) reduced seizures' frequency in one of two each. This first worldwide retrospective analysis of anticonvulsive therapy in NCBRS helps to treat epilepsy in NCBRS that mostly shows only initial response to anticonvulsive therapy, especially with LEV and VPA, but very rarely shows complete freedom of seizures in this, rather genetic than structural epilepsy.


Asunto(s)
Anticonvulsivantes/farmacología , Epilepsia/terapia , Deformidades Congénitas del Pie/terapia , Hipotricosis/terapia , Discapacidad Intelectual/terapia , Adolescente , Niño , Preescolar , Dieta Cetogénica , Electroencefalografía , Epilepsia/diagnóstico , Epilepsia/etiología , Epilepsia/fisiopatología , Facies , Femenino , Deformidades Congénitas del Pie/complicaciones , Deformidades Congénitas del Pie/diagnóstico , Deformidades Congénitas del Pie/fisiopatología , Humanos , Hipotricosis/complicaciones , Hipotricosis/diagnóstico , Hipotricosis/fisiopatología , Lactante , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/diagnóstico , Discapacidad Intelectual/fisiopatología , Masculino , Evaluación de Resultado en la Atención de Salud , Estudios Retrospectivos , Factores de Transcripción/genética , Estimulación del Nervio Vago
4.
Eur J Med Genet ; 63(3): 103739, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31421289

RESUMEN

The chromatin remodeling AT-Rich interaction domain containing 1B protein (ARID1B) also known as BAF-associated factor, 250-KD, B (BAF250B) codified by the ARID1B gene (MIM#614556), is a small subunit of the mammalian SWI/SNF or BAF complex, an ATP-dependent protein machinery which is able to activate or repress gene transcription, allowing protein access to histones through DNA relaxed conformation. ARID1B gene mutations have been associated with two hereditary syndromic conditions, namely Coffin-Siris (CSS, MIM#135900) and Nicolaides-Baraitser syndromes (NCBRS, MIM#601358), characterized by neurodevelopment delay, craniofacial dysmorphisms and skeletal anomalies. Furthermore, intellectual impairment and central nervous system (CNS) alterations, comprising abnormal corpus callosum, have been associated with mutations in this gene. Moreover, ARID1B anomalies resulted to be involved in neoplastic events and Hirschprung disease. Here we report on two monozygotic male twins, displaying clinical appearance strikingly resembling NCBRS and CSS phenotype, who resulted carriers of a novel 6q25.3 microdeletion, encompassing only part of the ARID1B gene. The deleted segment was not inherited from the only parent tested and afflicted the first exons of the gene, coding for protein disordered region. We also provide, for the first time, a review of previously published ARID1B mutated patients with NCBRS and CSS phenotype and a computer-assisted dysmorphology analysis of NCBRS and ARID1B related CSS individuals, through the Face2Gene suite, confirming the existence of highly overlapping facial gestalt of both conditions. The present findings indicate that ARID1B could be considered a contributing gene not only in CSS but also in NCBRS phenotype, although the main gene related to this latter condition is the SMARCA2 gene (MIM#600014), another component of the BAF complex. So, ARID1B study should be considered in such individuals.


Asunto(s)
Anomalías Múltiples/genética , Proteínas de Unión al ADN/genética , Cara/anomalías , Deformidades Congénitas del Pie/genética , Deformidades Congénitas de la Mano/genética , Hipotricosis/genética , Discapacidad Intelectual/genética , Micrognatismo/genética , Cuello/anomalías , Factores de Transcripción/genética , Gemelos Monocigóticos/genética , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/patología , Anomalías Múltiples/fisiopatología , Cara/diagnóstico por imagen , Cara/patología , Cara/fisiopatología , Facies , Deformidades Congénitas del Pie/diagnóstico por imagen , Deformidades Congénitas del Pie/patología , Deformidades Congénitas del Pie/fisiopatología , Deformidades Congénitas de la Mano/diagnóstico por imagen , Deformidades Congénitas de la Mano/patología , Deformidades Congénitas de la Mano/fisiopatología , Humanos , Hipotricosis/diagnóstico por imagen , Hipotricosis/patología , Hipotricosis/fisiopatología , Discapacidad Intelectual/diagnóstico por imagen , Discapacidad Intelectual/patología , Discapacidad Intelectual/fisiopatología , Masculino , Micrognatismo/diagnóstico por imagen , Micrognatismo/patología , Micrognatismo/fisiopatología , Mutación Missense , Cuello/diagnóstico por imagen , Cuello/patología , Cuello/fisiopatología , Fenotipo , Empalme del ARN , Eliminación de Secuencia
5.
Doc Ophthalmol ; 138(2): 153-160, 2019 04.
Artículo en Inglés | MEDLINE | ID: mdl-30710256

RESUMEN

PURPOSE: To investigate a very rare case of hypotrichosis with cone-rod dystrophy caused by a P-cadherin CDH3 mutation. METHODS: A 16-year-old Syrian girl was examined at age 9 and 14 years with an ophthalmological examination, fundus imaging, OCT and electrophysiological recordings (ERG and PERG). A disease-targeted gene panel sequencing was performed. RESULTS: Fundus images showed pigmentations at the posterior eye pole to the mid periphery, as well as vessel tortuosity. OCT images revealed a loss of the outer retinal segments and IS/OS in the central macula. The scotopic and photopic ERGs showed moderately reduced amplitudes at age 9 years that became severely reduced at age of 14 years. The PERG was undetectable at age 9 years. In color vision testing, protan-deutan confusion errors occurred. Gene panel analysis revealed one homozygous mutation in CDH3 (c.1508G>A; p.Arg503His). CONCLUSION: This case shows that a CDH3 mutation besides macula dystrophy can cause widespread cone-rod dystrophy with hypotrichosis without any other pathology besides hypoplastic nails. This points to a common pathway of hair growth and photoreceptor development that can be disturbed by a CDH3 mutation (c.1508G>A; p.Arg503His) located in the EC4 repeat region of the gene.


Asunto(s)
Cadherinas/genética , Distrofias de Conos y Bastones/genética , Hipotricosis/congénito , Degeneración Macular/genética , Mutación , Adolescente , Distrofias de Conos y Bastones/fisiopatología , Electrorretinografía , Femenino , Humanos , Hipotricosis/genética , Hipotricosis/fisiopatología , Degeneración Macular/fisiopatología , Retina/fisiopatología , Tomografía de Coherencia Óptica
7.
Clin Exp Optom ; 100(6): 583-589, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28122407

RESUMEN

PURPOSE: LATISSE is marketed for the treatment of hypotrichosis (loss of eyelashes), using a prostamide analogue and preserved with benzalkonium chloride, which is an effective preservative; however, it also causes irritation to the ocular surface. LATISSE is applied to the lid margin; however, with the blink, some solution may fall onto the ocular surface. The objective of this study was to assess the effects of LATISSE on the ocular surface over two months. METHODS: Non-dry eye participants interested in eyelash lengthening were invited to a prospective uncontrolled, open-label clinical study using LATISSE for two months. Eyelash length, subjective symptoms, tear film stability, osmolarity, ocular redness and intraocular pressure were evaluated at baseline (T0) and at one (T1) and two months (T2). RESULTS: Twenty-eight women (ages 18 to 29) entered the study. Fifteen completed the study with five who discontinued due to burning upon instillation and eight were lost to follow-up. Average eyelash length increased at each time (p < 0.001). Dryness, burning and grittiness remained low (less than 25/100) throughout the trial with dryness showing a significant change between T0 and T1 (p = 0.04), but not between T1 and T2 (p > 0.05). No difference (p > 0.05) was noted for the non-invasive break-up time, photochromametry or tear osmolarity. Intraocular pressure showed a decrease with time but translated to only a one to two mmHg change, which was not clinically relevant. CONCLUSIONS: LATISSE increases eyelash length within a short time (less than two months). Patients seeking eyelash enhancement options should be educated as to the use, precautions and any secondary effects, including the potential for discomfort upon instillation.


Asunto(s)
Antihipertensivos/administración & dosificación , Bimatoprost/administración & dosificación , Pestañas/efectos de los fármacos , Hipotricosis/tratamiento farmacológico , Administración Oftálmica , Adolescente , Adulto , Antihipertensivos/efectos adversos , Bimatoprost/efectos adversos , Síndromes de Ojo Seco/inducido químicamente , Dolor Ocular/inducido químicamente , Pestañas/fisiología , Femenino , Humanos , Hipotricosis/fisiopatología , Presión Intraocular/efectos de los fármacos , Soluciones Oftálmicas , Concentración Osmolar , Estudios Prospectivos , Encuestas y Cuestionarios , Lágrimas/química , Tonometría Ocular , Agudeza Visual/efectos de los fármacos , Adulto Joven
8.
Am J Med Genet A ; 170(7): 1754-62, 2016 07.
Artículo en Inglés | MEDLINE | ID: mdl-27112773

RESUMEN

The genetic basis of numerous intellectual disability (ID) syndromes has recently been identified by applying exome analysis on a research or clinical basis. There is significant clinical overlap of biologically related syndromes, as exemplified by Nicolaides-Baraitser (NCBRS) and Coffin-Siris (CSS) syndrome. Both result from mutations affecting the BAF (mSWI/SNF) complex and belong to the growing category of BAFopathies. In addition to the notable clinical overlap between these BAFopathies, heterogeneity exists for patients clinically diagnosed with one of these conditions. We report two teenagers with ID whose molecular diagnosis of a SMARC2A or ARID1B mutation, respectively, was established through clinical exome analysis. Interestingly, using only the information provided in a single clinically obtained facial photograph from each patient, the facial dysmorphology analysis detected similarities to facial patterns associated with NCBRS as the first suggestion for both individuals, followed by CSS as the second highest ranked in the individual with the ARID1B mutation. Had this information been available to the laboratory performing the exome analysis, it could have been utilized during the variant analysis and reporting process, in conjunction with the written summary provided with each test requisition. While the available massive parallel sequencing technology, variant calling and variant interpretation are constantly evolving, clinical information remains critical for this diagnostic process. When trio analysis is not feasible, additional diagnostic tools may become particularly valuable. Facial dysmorphology analysis data may supplement the clinical phenotype summary and provide data independent of the clinician's personal experience and bias. © 2016 Wiley Periodicals, Inc.


Asunto(s)
Anomalías Múltiples/diagnóstico , Anomalías Craneofaciales/diagnóstico , Proteínas de Unión al ADN/genética , Cara/anomalías , Deformidades Congénitas del Pie/diagnóstico , Deformidades Congénitas de la Mano/diagnóstico , Hipotricosis/diagnóstico , Discapacidad Intelectual/diagnóstico , Micrognatismo/diagnóstico , Atrofia Muscular/diagnóstico , Cuello/anomalías , Factores de Transcripción/genética , Anomalías Múltiples/genética , Anomalías Múltiples/fisiopatología , Adolescente , Anomalías Craneofaciales/genética , Anomalías Craneofaciales/fisiopatología , Exoma/genética , Cara/fisiopatología , Facies , Femenino , Deformidades Congénitas del Pie/genética , Deformidades Congénitas del Pie/fisiopatología , Deformidades Congénitas de la Mano/genética , Deformidades Congénitas de la Mano/fisiopatología , Humanos , Hipotricosis/genética , Hipotricosis/fisiopatología , Discapacidad Intelectual/genética , Discapacidad Intelectual/fisiopatología , Masculino , Micrognatismo/genética , Micrognatismo/fisiopatología , Atrofia Muscular/genética , Atrofia Muscular/fisiopatología , Mutación , Cuello/fisiopatología , Proteínas Nucleares/genética , Patología Molecular , Fenotipo
9.
Aesthet Surg J ; 36(2): 221-8, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26691738

RESUMEN

BACKGROUND: Patient-reported outcome (PRO) measures have been used to assess treatment benefit in a variety of therapeutic areas and are now becoming increasingly important in aesthetic research. OBJECTIVES: The objective of the current study was to develop and validate a new PRO measure (Eyelash Satisfaction Questionnaire [ESQ]) to assess satisfaction with eyelash prominence. METHODS: The content of the questionnaire (including conceptual framework and questionnaire items) was generated by review of literature, participant interviews, and expert opinion. Cognitive interviews were conducted to pilot test the questionnaire. Psychometric properties of the questionnaire were examined in a combined sample of participants (n = 970) completing Internet- (n = 909) and paper-based (n = 61) versions. Item- and domain-level properties were examined using modern and classical psychometrics. RESULTS: Content-based analysis of qualitative data demonstrated the presence of 3 distinct domains (Length, Fullness, Overall Satisfaction; Confidence, Attractiveness, and Professionalism; and Daily Routine). Initial confirmatory factor analysis (CFA) results of 23 items revealed insufficient model-data fit (comparative fit index [CFI] of 0.86 and a non-normed fit index [NNFI] of 0.82). A revised model using 9 items (3 per domain) achieved appropriate fit (CFI of 0.99 and NNFI of 0.97). Analyses revealed measurement equivalence across the Internet- and paper-based versions. The 3 ESQ domains had strong internal consistency reliability (Cronbach's α [range] = 0.919-0.976) and adequate convergent and discriminant validity. CONCLUSIONS: The ESQ was found to be a reliable and valid PRO measure for assessing satisfaction with eyelash prominence. LEVEL OF EVIDENCE 3: Therapeutic.


Asunto(s)
Bimatoprost/uso terapéutico , Estética , Pestañas/efectos de los fármacos , Hipotricosis/tratamiento farmacológico , Satisfacción del Paciente , Encuestas y Cuestionarios , Adulto , Anciano , California , Chicago , Cognición , Comprensión , Pestañas/crecimiento & desarrollo , Femenino , Grupos Focales , Humanos , Hipotricosis/diagnóstico , Hipotricosis/fisiopatología , Masculino , Persona de Mediana Edad , Psicometría , Reproducibilidad de los Resultados , Resultado del Tratamiento , Adulto Joven
10.
Dermatol Online J ; 21(7)2015 Jul 15.
Artículo en Portugués | MEDLINE | ID: mdl-26436976

RESUMEN

Graham-Little-Piccardi-Lassueur syndrome is a rare lichenoid dermatosis. It is characterized by the triad of scarring alopecia of the scalp, alopecia of the axilla and or groin, and keratotic follicular papules of the body. The present paper reports on two cases affecting young women. Histopathological findings suggest the disorder represents a generalized form of lichen planus follicularis.


Asunto(s)
Alopecia/patología , Hipotricosis/patología , Liquen Plano/patología , Adulto , Alopecia/complicaciones , Alopecia/fisiopatología , Biopsia con Aguja , Brasil , Femenino , Humanos , Hipotricosis/complicaciones , Hipotricosis/fisiopatología , Inmunohistoquímica , Liquen Plano/complicaciones , Liquen Plano/fisiopatología , Pronóstico , Enfermedades Raras , Síndrome
12.
Neuropharmacology ; 80: 83-94, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24434855

RESUMEN

Cognitive disorders (CDs) are a heterogeneous group of disorders for which the genetic foundations are rapidly being uncovered. The large number of CD-associated gene mutations presents an opportunity to identify common mechanisms of disease as well as molecular processes that are of key importance to human cognition. Given the disproportionately high number of epigenetic genes associated with CD, epigenetic regulation of gene transcription is emerging as a process of major importance in cognition. The cognate protein products of these genes often co-operate in shared protein complexes or pathways, which is reflected in similarities between the neurodevelopmental phenotypes corresponding to these mutant genes. Here we provide an overview of the genes associated with CDs, and highlight some of the epigenetic regulatory complexes involving multiple CD genes. Such common gene networks may provide a handle for designing therapeutic interventions applicable to a number of cognitive disorders with variable genetic etiology.


Asunto(s)
Encéfalo/metabolismo , Trastornos del Conocimiento/metabolismo , Cognición , Epigénesis Genética , Modelos Biológicos , Neuronas/metabolismo , Anomalías Múltiples/genética , Anomalías Múltiples/metabolismo , Anomalías Múltiples/fisiopatología , Animales , Encéfalo/enzimología , Ensamble y Desensamble de Cromatina , Deleción Cromosómica , Cromosomas Humanos Par 9/genética , Cromosomas Humanos Par 9/metabolismo , Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/genética , Anomalías Craneofaciales/genética , Anomalías Craneofaciales/metabolismo , Anomalías Craneofaciales/fisiopatología , Cara/anomalías , Cara/fisiopatología , Facies , Deformidades Congénitas del Pie/genética , Deformidades Congénitas del Pie/metabolismo , Deformidades Congénitas del Pie/fisiopatología , Regulación de la Expresión Génica , Deformidades Congénitas de la Mano/genética , Deformidades Congénitas de la Mano/metabolismo , Deformidades Congénitas de la Mano/fisiopatología , Cardiopatías Congénitas/genética , Cardiopatías Congénitas/metabolismo , Cardiopatías Congénitas/fisiopatología , Humanos , Hipotricosis/genética , Hipotricosis/metabolismo , Hipotricosis/fisiopatología , Discapacidad Intelectual/genética , Discapacidad Intelectual/metabolismo , Discapacidad Intelectual/fisiopatología , Micrognatismo/genética , Micrognatismo/metabolismo , Micrognatismo/fisiopatología , Mutación , Cuello/anomalías , Cuello/fisiopatología , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , Neuronas/enzimología
13.
Aesthet Surg J ; 33(6): 789-98, 2013 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-23873891

RESUMEN

BACKGROUND: Hypotrichosis of the eyelashes may negatively influence an individual's self-perception and appearance. Assessing the impact of treatment from a patient's perspective may be particularly relevant in trials of aesthetic agents. Once-daily dermal (topically applied) administration of bimatoprost ophthalmic solution 0.03% has been associated with increased eyelash prominence (ie, length, thickness, darkness). OBJECTIVES: The authors assess patient-reported outcomes (PRO) after treatment with bimatoprost for hypotrichosis of the eyelashes. METHODS: In this multicenter, double-masked, randomized, vehicle-controlled, parallel clinical trial, 4 PRO questionnaires were distributed to 278 patients (bimatoprost [n = 137] and vehicle [n = 141]). The primary PRO questionnaire was the 23-item Eyelash Satisfaction Questionnaire (ESQ), which measured satisfaction in 3 domains: length, fullness, and overall satisfaction (LFOS); confidence, attractiveness, and professionalism (CAP); and impact on daily routine (DR). RESULTS: By week 16, the bimatoprost group reported significantly greater improvements from baseline on all ESQ items (P ≤ .0433). These improvements were sustained through the 4-week posttreatment study visit. Patient satisfaction was significantly greater in the bimatoprost group than in the vehicle group for all 3 domains: LFOS (weeks 8-20; P ≤ .0052), CAP (weeks 12-20; P < .0001), and DR (weeks 16 and 20; P ≤ .01). CONCLUSIONS: The bimatoprost group reported significantly greater levels of positive patient outcomes and satisfaction than the vehicle group across all 23 questions and all 3 domains of the primary PRO questionnaire. These results support the effectiveness, as measured by objective measures and PRO, of once-daily bimatoprost ophthalmic solution 0.03% at producing more prominent eyelashes in adults.


Asunto(s)
Amidas/uso terapéutico , Cloprostenol/análogos & derivados , Pestañas/efectos de los fármacos , Hipotricosis/tratamiento farmacológico , Administración Tópica , Adulto , Anciano , Amidas/administración & dosificación , Bimatoprost , Imagen Corporal , Canadá , Cloprostenol/administración & dosificación , Cloprostenol/uso terapéutico , Costo de Enfermedad , Método Doble Ciego , Pestañas/crecimiento & desarrollo , Femenino , Humanos , Hipotricosis/fisiopatología , Hipotricosis/psicología , Masculino , Persona de Mediana Edad , Soluciones Oftálmicas , Satisfacción del Paciente , Autoimagen , Encuestas y Cuestionarios , Factores de Tiempo , Resultado del Tratamiento , Estados Unidos , Adulto Joven
14.
J Invest Dermatol ; 132(10): 2332-2341, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22696062

RESUMEN

P-cadherin is a key component of epithelial adherens junctions, and it is prominently expressed in the hair follicle (HF) matrix. Loss-of-function mutations in CDH3, which encodes P-cadherin, result in hypotrichosis with juvenile macular dystrophy (HJMD), an autosomal recessive disorder featuring sparse and short hair. Here, we attempted to recapitulate some aspects of HJMD in vitro by transfecting normal, organ-cultured human scalp HFs with lipofectamine and CDH3-specific or scrambled control siRNAs. As in HJMD patients, P-cadherin silencing inhibited hair shaft growth, prematurely induced HF regression (catagen), and inhibited hair matrix keratinocyte proliferation. In situ, membrane ß-catenin expression and transcription of the ß-catenin target gene, axin2, were significantly reduced, whereas glycogen synthase kinase 3 ß (GSK3ß) and phospho-ß-catenin immunoreactivity were increased. These effects were partially reversed by inhibiting GSK3ß. P-cadherin silencing reduced the expression of the anagen-promoting growth factor, IGF-1, whereas that of transforming growth factor ß 2 (TGFß2; catagen promoter) was enhanced. Neutralizing TGFß antagonized the catagen-promoting effects of P-cadherin silencing. In summary, we introduce human HFs as an attractive preclinical model for studying the functions of P-cadherin in human epithelial biology and pathology. This model demonstrates that cadherins can be successfully knocked down in an intact human organ in vitro, and shows that P-cadherin is needed for anagen maintenance by regulating canonical Wnt signaling and suppressing TGFß2.


Asunto(s)
Cadherinas/metabolismo , Ciclo Celular/fisiología , Proliferación Celular , Cabello/crecimiento & desarrollo , Cabello/metabolismo , Factor de Crecimiento Transformador beta2/metabolismo , Vía de Señalización Wnt/fisiología , Adulto , Cadherinas/efectos de los fármacos , Cadherinas/genética , Células Cultivadas , Comorbilidad , Femenino , Silenciador del Gen/efectos de los fármacos , Cabello/citología , Folículo Piloso/citología , Folículo Piloso/crecimiento & desarrollo , Humanos , Hipotricosis/epidemiología , Hipotricosis/etiología , Hipotricosis/fisiopatología , Técnicas In Vitro , Degeneración Macular/epidemiología , Degeneración Macular/etiología , Degeneración Macular/fisiopatología , Masculino , Persona de Mediana Edad , ARN Interferente Pequeño/farmacología , Transfección
15.
Clin Dysmorphol ; 20(1): 38-41, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20802310

RESUMEN

Nicolaides-Baraitser syndrome is a rare clinical condition characterized by mental retardation with impairment of expressive language, short stature, microcephaly, sparse hair, typical facial dysmorphisms, and interphalangeal joint swellings. To date 24 cases have been reported, most of them being sporadic. The genetic background of Nicolaides-Baraitser syndrome is unclear in terms of cause and mode of inheritance, one of the more probable explanations is de novo mutation of a dominant gene. Some reported patients presented autistic features, although in none of these patients was the diagnosis of autism spectrum disorder formally made. We describe two unrelated patients with clinical features suggesting Nicolaides-Baraitser syndrome and, in addition, autism spectrum disorder is defined by the presence of the three cardinal core features: qualitative impairments in social, communicative, and behavioral development.


Asunto(s)
Trastornos Generalizados del Desarrollo Infantil/complicaciones , Niño , Trastornos Generalizados del Desarrollo Infantil/fisiopatología , Preescolar , Cognición/fisiología , Facies , Femenino , Deformidades Congénitas del Pie/complicaciones , Deformidades Congénitas del Pie/fisiopatología , Humanos , Hipotricosis/complicaciones , Hipotricosis/fisiopatología , Lactante , Recién Nacido , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/fisiopatología , Embarazo
16.
Arch Dermatol Res ; 302(9): 701-3, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20140736

RESUMEN

Mutations in CDH3 gene, encoding P-cadherin, are responsible for hypotrichosis with juvenile macular dystrophy (HJMD), which is a rare autosomal recessive disorder. The HJMD is characterized by congenital sparse hair on scalp and progressive severe degenerative changes of the retinal macula which leads to variable degrees of blindness. The present study reports a large consanguineous Pakistani family with six individuals affected with HJMD. Genotyping using polymorphic microsatellite markers showed linkage of the family to CDH3 gene on chromosome 16q22.1. Sequence analysis of the CDH3 gene revealed a novel splice site mutation (c.IVS10-1 G â†’ A) in intron 10, which leads to skipping of exon 11 and probably synthesizing a non-functional premature truncated protein.


Asunto(s)
Cadherinas/genética , Intrones/genética , Mutación/genética , Sitios de Empalme de ARN/genética , Cadherinas/metabolismo , Cromosomas Humanos Par 16/genética , Consanguinidad , Análisis Mutacional de ADN , Femenino , Genotipo , Folículo Piloso/patología , Humanos , Hipotricosis/congénito , Hipotricosis/epidemiología , Hipotricosis/genética , Hipotricosis/patología , Hipotricosis/fisiopatología , Degeneración Macular/epidemiología , Degeneración Macular/genética , Degeneración Macular/patología , Degeneración Macular/fisiopatología , Masculino , Pakistán , Linaje
18.
Hum Mol Genet ; 18(15): 2839-50, 2009 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-19429912

RESUMEN

Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome. Here, we clarify the role of SOX18 in the vascular dysfunction in HLT by ultrastructural, immunofluorescence, molecular and functional analysis of vascular anomalies in embryos of the naturally occurring Sox18-mutant mouse strain ragged-opossum (Ra(Op)). Early genesis and patterning of vasculature was unimpaired in Ra(Op) embryos, but surface capillaries became enlarged from 12.5 dpc and embryos developed massive surface hemorrhage by 14.5 dpc. Large focal breaches in the endothelial barrier were observed, in addition to endothelial hyperplasia associated with impaired pericyte recruitment to the microvasculature. Expression of the genes encoding the endothelial factors MMP7, IL7R and N-cadherin was reduced in Ra(Op) embryos, suggesting that these are downstream targets of SOX18. Together, our results indicate that vascular anomalies in HLT arise from defects in regulation of genes required for the acquisition of structural integrity during microvascular maturation.


Asunto(s)
Vasos Sanguíneos/fisiopatología , Hipotricosis/metabolismo , Linfedema/metabolismo , Factores de Transcripción SOXF/metabolismo , Telangiectasia/metabolismo , Animales , Vasos Sanguíneos/anomalías , Vasos Sanguíneos/embriología , Vasos Sanguíneos/metabolismo , Modelos Animales de Enfermedad , Humanos , Hipotricosis/embriología , Hipotricosis/genética , Hipotricosis/fisiopatología , Linfedema/embriología , Linfedema/genética , Linfedema/fisiopatología , Masculino , Ratones , Ratones Endogámicos DBA , Factores de Transcripción SOXF/genética , Telangiectasia/embriología , Telangiectasia/genética , Telangiectasia/fisiopatología
19.
Arch Dermatol Res ; 301(5): 391-3, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18820939

RESUMEN

Autosomal recessive hypotrichosis simplex (ARHS) manifests with paucity of hair appearing during early childhood. We assessed four affected families. We initially genotyped three of these families for a panel of microsatellite markers spanning all ARHS-associated loci and obtained data suggesting linkage to 3q27, encompassing LIPH, which had previously been shown to be associated with ARHS. Accordingly, a homozygous duplication mutation in exon 2 of this gene (c.280_369dup; p.Gly94_Lys123dup) was found to segregate with the disease in all the families. Through the identification of the first duplication mutation in the human LIPH gene, we provide further evidence supporting a role for the phospholipase signalling pathway in hair growth and differentiation.


Asunto(s)
Árabes , Trastornos de los Cromosomas/genética , Duplicación de Gen , Folículo Piloso/metabolismo , Hipotricosis/genética , Lipasa/genética , Niño , Trastornos de los Cromosomas/enzimología , Trastornos de los Cromosomas/patología , Trastornos de los Cromosomas/fisiopatología , Cromosomas Humanos Par 3 , Análisis Mutacional de ADN , Exones/genética , Genes Recesivos , Predisposición Genética a la Enfermedad , Cabello/anomalías , Cabello/crecimiento & desarrollo , Cabello/patología , Folículo Piloso/crecimiento & desarrollo , Folículo Piloso/patología , Humanos , Hipotricosis/enzimología , Hipotricosis/patología , Hipotricosis/fisiopatología , Israel , Lipasa/metabolismo , Repeticiones de Microsatélite/genética , Linaje , Polimorfismo Genético , Turquía
20.
J Invest Dermatol ; 129(2): 438-48, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18987668

RESUMEN

The primary cilium is a microtubule-based organelle implicated as an essential component of a number of signaling pathways. It is present on cells throughout the mammalian body; however, its functions in most tissues remain largely unknown. Herein we demonstrate that primary cilia are present on cells in murine skin and hair follicles throughout morphogenesis and during hair follicle cycling in postnatal life. Using the Cre-lox system, we disrupted cilia assembly in the ventral dermis and evaluated the effects on hair follicle development. Mice with disrupted dermal cilia have severe hypotrichosis (lack of hair) in affected areas. Histological analyses reveal that most follicles in the mutants arrest at stage 2 of hair development and have small or absent dermal condensates. This phenotype is reminiscent of that seen in the skin of mice lacking Shh or Gli2. In situ hybridization and quantitative RT-PCR analysis indicates that the hedgehog pathway is downregulated in the dermis of the cilia mutant hair follicles. Thus, these data establish cilia as a critical signaling component required for normal hair morphogenesis and suggest that this organelle is needed on cells in the dermis for reception of signals such as sonic hedgehog.


Asunto(s)
Cilios/fisiología , Folículo Piloso/citología , Folículo Piloso/crecimiento & desarrollo , Proteínas Hedgehog/metabolismo , Hipotricosis/fisiopatología , Animales , Dermis/citología , Proteínas Hedgehog/genética , Hipotricosis/metabolismo , Hipotricosis/patología , Integrasas/genética , Factores de Transcripción de Tipo Kruppel/genética , Factores de Transcripción de Tipo Kruppel/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Fenotipo , Transducción de Señal/fisiología , Proteínas Wnt/metabolismo , Proteína Gli2 con Dedos de Zinc
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