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1.
Am J Hum Genet ; 102(6): 1090-1103, 2018 06 07.
Artículo en Inglés | MEDLINE | ID: mdl-29805044

RESUMEN

The 6%-9% risk of an untoward outcome previously established by Warburton for prenatally detected de novo balanced chromosomal rearrangements (BCRs) does not account for long-term morbidity. We performed long-term follow-up (mean 17 years) of a registry-based nationwide cohort of 41 individuals carrying a prenatally detected de novo BCR with normal first trimester screening/ultrasound scan. We observed a significantly higher frequency of neurodevelopmental and/or neuropsychiatric disorders than in a matched control group (19.5% versus 8.3%, p = 0.04), which was increased to 26.8% upon clinical follow-up. Chromosomal microarray of 32 carriers revealed no pathogenic imbalances, illustrating a low prognostic value when fetal ultrasound scan is normal. In contrast, mate-pair sequencing revealed disrupted genes (ARID1B, NPAS3, CELF4), regulatory domains of known developmental genes (ZEB2, HOXC), and complex BCRs associated with adverse outcomes. Seven unmappable autosomal-autosomal BCRs with breakpoints involving pericentromeric/heterochromatic regions may represent a low-risk group. We performed independent phenotype-aware and blinded interpretation, which accurately predicted benign outcomes (specificity = 100%) but demonstrated relatively low sensitivity for prediction of the clinical outcome in affected carriers (sensitivity = 45%-55%). This sensitivity emphasizes the challenges associated with prenatal risk prediction for long-term morbidity in the absence of phenotypic data given the still immature annotation of the morbidity genome and poorly understood long-range regulatory mechanisms. In conclusion, we upwardly revise the previous estimates of Warburton to a morbidity risk of 27% and recommend sequencing of the chromosomal breakpoints as the first-tier diagnostic test in pregnancies with a de novo BCR.


Asunto(s)
Aberraciones Cromosómicas , Diagnóstico Prenatal/métodos , Puntos de Rotura del Cromosoma , Estudios de Cohortes , Secuencia Conservada/genética , Evolución Molecular , Femenino , Genoma Humano , Humanos , Cariotipificación , Embarazo , ARN Largo no Codificante/genética , Factores de Riesgo , Análisis de Secuencia de ADN , Factores de Tiempo
2.
Scand J Clin Lab Invest ; 78(4): 293-300, 2018 07.
Artículo en Inglés | MEDLINE | ID: mdl-29661028

RESUMEN

In vitro expanded adipose-derived stromal cells (ASCs) are a useful resource for tissue regeneration. Translation of small-scale autologous cell production into a large-scale, allogeneic production process for clinical applications necessitates well-chosen raw materials and cell culture platform. We compare the use of clinical-grade human platelet lysate (hPL) and fetal bovine serum (FBS) as growth supplements for ASC expansion in the automated, closed hollow fibre quantum cell expansion system (bioreactor). Stromal vascular fractions were isolated from human subcutaneous abdominal fat. In average, 95 × 106 cells were suspended in 10% FBS or 5% hPL medium, and loaded into a bioreactor coated with cryoprecipitate. ASCs (P0) were harvested, and 30 × 106 ASCs were reloaded for continued expansion (P1). Feeding rate and time of harvest was guided by metabolic monitoring. Viability, sterility, purity, differentiation capacity, and genomic stability of ASCs P1 were determined. Cultivation of SVF in hPL medium for in average nine days, yielded 546 × 106 ASCs compared to 111 × 106 ASCs, after 17 days in FBS medium. ASCs P1 yields were in average 605 × 106 ASCs (PD [population doublings]: 4.65) after six days in hPL medium, compared to 119 × 106 ASCs (PD: 2.45) in FBS medium, after 21 days. ASCs fulfilled ISCT criteria and demonstrated genomic stability and sterility. The use of hPL as a growth supplement for ASCs expansion in the quantum cell expansion system provides an efficient expansion process compared to the use of FBS, while maintaining cell quality appropriate for clinical use. The described process is an obvious choice for manufacturing of large-scale allogeneic ASC products.


Asunto(s)
Tejido Adiposo/citología , Reactores Biológicos , Plaquetas/metabolismo , Técnicas de Cultivo de Célula/métodos , Células Madre Mesenquimatosas/citología , Adulto , Diferenciación Celular , Proliferación Celular , Femenino , Inestabilidad Genómica , Humanos , Lactatos/metabolismo , Masculino , Células Madre Mesenquimatosas/metabolismo , Persona de Mediana Edad , Fenotipo , Factores de Tiempo
3.
Scand J Clin Lab Invest ; 76(2): 93-104, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26878874

RESUMEN

BACKGROUND: The utility of mesenchymal stromal cells (MSCs) in therapeutic applications for regenerative medicine has gained much attention. Clinical translation of MSC-based approaches requires in vitro culture-expansion to achieve a sufficient number of cells. The ideal cell culture medium should be devoid of any animal derived components. We have evaluated whether human Platelet Lysate (hPL) could be an attractive alternative to animal supplements. METHODS: MSCs from bone marrow (BMSCs) and adipose tissue-derived stromal cells (ASCs) obtained from three donors were culture expanded in three different commercially available hPL fulfilling good manufacturing practice criteria for clinical use. BMSCs and ASCs cultured in Minimum Essential Medium Eagle-alpha supplemented with 5% PLT-Max (Mill Creek), Stemulate™ PL-S and Stemulate™ PL-SP (COOK General Biotechnology) were compared to standard culture conditions with 10% fetal bovine serum (FBS). Cell morphology, proliferation, phenotype, genomic stability, and differentiation potential were analyzed. RESULTS: Regardless of manufacturer, BMSCs and ASCs cultured in hPL media showed a significant increase in proliferation capacity compared to FBS medium. In general, the immunophenotype of both BMSCs and ASCs fulfilled International Society for Cellular Therapy (ISCT) criteria after hPL media expansion. Comparative genomic hybridization measurements demonstrated no unbalanced chromosomal rearrangements for BMSCs or ASCs cultured in hPL media or FBS medium. The BMSCs and ASCs could differentiate into osteogenic, adipogenic, or chondrogenic lineages in all four culture conditions. CONCLUSION: All three clinically approved commercial human platelet lysates accelerated proliferation of BMSCs and ASCs and the cells meet the ISCT mesenchymal phenotypic requirements without exhibiting chromosomal aberrations.


Asunto(s)
Plaquetas/química , Células Madre Mesenquimatosas/fisiología , Tejido Adiposo/citología , Adulto , Células de la Médula Ósea/fisiología , Técnicas de Cultivo de Célula , Diferenciación Celular , Extractos Celulares , Proliferación Celular , Forma de la Célula , Hibridación Genómica Comparativa , Medios de Cultivo/química , Femenino , Inestabilidad Genómica , Humanos , Masculino , Persona de Mediana Edad , Cultivo Primario de Células , Adulto Joven
4.
Am J Med Genet A ; 167A(11): 2731-6, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26109418

RESUMEN

Nervous system development is highly dependent on the function of microtubules, which are assembled from tubulin heterodimers containing several α- and ß-tubulin isotypes encoded by separate genes. A spectrum of neurological disorders with malformations of the central nervous system has recently been associated with missense mutations in this group of genes. Here, we report two patients, monozygotic twins, carrying a de novo 0.32 Mb deletion of chromosome 16q24.3 including the TUBB3 gene. The patients presented with global developmental delay, mild facial dysmorphism, secondary microcephaly, and mild spastic diplegia. Cerebral magnetic resonance imaging of the patients did not reveal cortical malformations, malformations of the corticospinal tracts, basal ganglia, corpus callosum, or optic nerves. This observation is in contrast to the group of neurological disorders that are associated with heterozygous missense mutations in genes encoding different neuronal α- and ß-tubulin isotypes, termed tubulinopathies. On the background of current knowledge regarding the function and genotype-phenotype correlations of mutations in the neuronal tubulin isotypes, the clinical and diagnostic findings in these patients are discussed. To our knowledge, this is the first report of patients with a de novo deletion of the TUBB3 gene. The lack of cortical or other cerebral malformations supports the current hypothesis that TUBB3-related tubulinopathies are caused by altered protein function.


Asunto(s)
Emparejamiento Base/genética , Encéfalo/anomalías , Discapacidades del Desarrollo/genética , Facies , Eliminación de Secuencia , Tubulina (Proteína)/genética , Gemelos Monocigóticos/genética , Cromosomas Humanos Par 16/genética , Hibridación Genómica Comparativa , Humanos , Lactante , Recién Nacido , Imagen por Resonancia Magnética
5.
Lancet ; 382(9898): 1113-20, 2013 Sep 28.
Artículo en Inglés | MEDLINE | ID: mdl-24075051

RESUMEN

BACKGROUND: Autologous fat grafting is increasingly used in reconstructive surgery. However, resorption rates ranging from 25% to 80% have been reported. Therefore, methods to increase graft viability are needed. Here, we report the results of a triple-blind, placebo-controlled trial to compare the survival of fat grafts enriched with autologous adipose-derived stem cells (ASCs) versus non-enriched fat grafts. METHODS: Healthy participants underwent two liposuctions taken 14 days apart: one for ASC isolation and ex-vivo expansion, and another for the preparation of fat grafts. Two purified fat grafts (30 mL each) taken from the second liposuction were prepared for each participant. One graft was enriched with ASCs (20 × 10(6) cells per mL fat), and another graft without ASC enrichment served as a control. The fat grafts were injected subcutaneously as a bolus to the posterior part of the right and left upper arm according to the randomisation sequence. The volumes of injected fat grafts were measured by MRI immediately after injection and after 121 days before surgical removal. The primary goal was to compare the residual graft volumes of ASC-enriched grafts with those of control grafts. This study is registered at www.clinicaltrialsregister.eu, number 2010-023006-12. FINDINGS: 13 participants were enrolled, three of whom were excluded. Compared with the control grafts, the ASC-enriched fat grafts had significantly higher residual volumes: 23·00 (95% CI 20·57-25·43) cm(3) versus 4·66 (3·16-6·16) cm(3) for the controls, corresponding to 80·9% (76·6-85·2) versus 16·3% (11·1-21·4) of the initial volumes, respectively (p<0·0001). The difference between the groups was 18·34 (95% CI 15·70-20·98) cm(3), equivalent to 64·6% (57·1-72·1; p<0·0001). No serious adverse events were noted. INTERPRETATION: The procedure of ASC-enriched fat grafting had excellent feasibility and safety. These promising results add significantly to the prospect of stem cell use in clinical settings, and indicate that ASC graft enrichment could render lipofilling a reliable alternative to major tissue augmentation, such as breast surgery, with allogeneic material or major flap surgery. FUNDING: Danish Cancer Society, Centre of Head and Orthopaedics Rigshospitalet, and Moalem Weitemeyer Bendtsen.


Asunto(s)
Adipocitos/trasplante , Tejido Adiposo/trasplante , Trasplante de Células Madre/métodos , Adolescente , Adulto , Brazo , Estudios de Factibilidad , Femenino , Supervivencia de Injerto/fisiología , Humanos , Lipectomía/métodos , Masculino , Persona de Mediana Edad , Trasplante Autólogo , Adulto Joven
6.
Am J Med Genet A ; 164A(5): 1277-83, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24664804

RESUMEN

Proximal deletions of the long arm of chromosome 13 have been reported only rarely. Here we present three unrelated patients with heterozygous, apparently de novo deletions encompassing 13q12.3. The patients present with moderate demonstrated or apparent intellectual disability, postnatal microcephaly, and eczema/atopic dermatitis as the predominant symptoms. In addition, they had pronounced feeding difficulties in early infancy. They displayed similar facial features such as malar flattening, a prominent nose with underdeveloped alae nasi, a smooth philtrum, and a thin vermillion of the upper lip. The proximal and distal breakpoints were clustered and the deletions spanned from 1.4 to 1.7 Mb, comprising at least 11 RefSeq genes. However, heterozygous deletions partially overlapping those observed in the present patients have been described in healthy parents of patients with Peters-Plus syndrome, an autosomal recessive disorder caused by inactivation of the B3GALTL gene. We therefore propose that the critical region of the 13q12.3 microdeletion syndrome contains only three genes, namely, KATNAL1, HMGB1, and LINC00426, a non-protein coding RNA. The KATNAL1 protein belongs to a family of microtubule severing enzymes that have been implicated in CNS plasticity in experimental models, but little is known about its function in humans. The HMGB1 protein is an evolutionarily conserved chromatin-associated protein involved in many biologically important processes. In summary, we propose that microdeletion 13q12.3 represents a novel clinically recognizable condition and that the microtubule severing gene KATNAL1 and the chromatin-associated gene HMGB1 are candidate genes for intellectual disability inherited in an autosomal dominant pattern.


Asunto(s)
Anomalías Múltiples/diagnóstico , Anomalías Múltiples/genética , Adenosina Trifosfatasas/genética , Deleción Cromosómica , Cromosomas Humanos Par 13 , Proteína HMGB1/genética , Fenotipo , Adolescente , Niño , Preescolar , Hibridación Genómica Comparativa , Dermatitis Atópica , Eccema , Facies , Femenino , Humanos , Discapacidad Intelectual , Cariotipificación , Katanina , Masculino , Microcefalia
7.
Cytotherapy ; 15(9): 1086-97, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23602579

RESUMEN

BACKGROUND AIMS: Because of an increasing focus on the use of adipose-derived stem cells (ASCs) in clinical trials, the culture conditions for these cells are being optimized. We compared the proliferation rates and chromosomal stability of ASCs that had been cultured in Dulbecco's modified Eagle's Medium (DMEM) supplemented with either pooled human platelet lysate (pHPL) or clinical-grade fetal bovine serum (FBS) (DMEM(pHPL) versus DMEM(FBS)). METHODS: ASCs from four healthy donors were cultured in either DMEM(pHPL) or DMEM(FBS), and the population doubling time (PDT) was calculated. ASCs from two of the donors were expanded in DMEM(pHPL) or DMEM(FBS) and cultured for the final week before harvesting with or without the addition of vascular endothelial growth factor. We assessed the chromosomal stability (through the use of array comparative genomic hybridization), the expression of ASC and endothelial surface markers and the differentiation and angiogenic potential of these cells. RESULTS: The ASCs that were cultured in pHPL exhibited a significantly shorter PDT of 29.6 h (95% confidence interval, 22.3-41.9 h) compared with those cultured in FBS, for which the PDT was 123.9 h (95% confidence interval, 95.6-176.2 h). Comparative genomic hybridization analyses revealed no chromosomal aberrations. Cell differentiation, capillary structure formation and cell-surface marker expression were generally unaffected by the type of medium supplement that was used or by the addition of vascular endothelial growth factor. CONCLUSIONS: We observed that the use of pHPL as a growth supplement for ASCs facilitated a significantly higher proliferation rate compared with FBS without compromising genomic stability or differentiation capacity.


Asunto(s)
Tejido Adiposo/fisiología , Plaquetas/metabolismo , Inestabilidad Cromosómica/genética , Neovascularización Fisiológica/fisiología , Suero/metabolismo , Células Madre/fisiología , Tejido Adiposo/metabolismo , Animales , Bovinos , Técnicas de Cultivo de Célula/métodos , Diferenciación Celular/fisiología , Proliferación Celular , Células Cultivadas , Femenino , Humanos , Células Madre/metabolismo , Factor A de Crecimiento Endotelial Vascular/metabolismo
8.
Am J Med Genet A ; 161A(7): 1594-8, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-23704076

RESUMEN

We report on three males with de novo overlapping 7.5, 9.8, and 10 Mb duplication of chromosome 20q11.2. Together with another patient previously published in the literature with overlapping 20q11 microduplication, we show that such patients display common clinical features including metopic ridging/trigonocephaly, developmental delay, epicanthal folds, and short hands. The duplication comprised the ASXL1 gene, in which de novo heterozygous nonsense or truncating mutations have recently been reported in patients with Borhing-Opitz syndrome. Because of craniofacial features in common with Borhing-Opitz syndrome, in particular metopic ridging/trigonocephaly, we suggest that duplication of ASXL1 contributes to the phenotype. These observations suggest a novel microduplication syndrome, and reporting of additional patients with molecular characterization will allow more detailed genotype-phenotype correlations.


Asunto(s)
Craneosinostosis/genética , Proteínas Represoras/genética , Trisomía/genética , Niño , Preescolar , Cromosomas Humanos Par 20/genética , Discapacidades del Desarrollo/genética , Femenino , Deformidades Congénitas de la Mano/genética , Heterocigoto , Humanos , Lactante , Discapacidad Intelectual/genética , Masculino , Mosaicismo , Mutación , Embarazo , Síndrome
9.
Am J Med Genet A ; 158A(8): 1832-6, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22753084

RESUMEN

Array comparative genomic hybridization has led to the identification of new syndromes by identifying genomic imbalances not detectable by standard karyotyping methods and by allowing correlations with physical findings. Deletions in the 17p13.1 region have been reported in patients with dysmorphic features and developmental delay but a consistent phenotype has yet to emerge. This report describes two unrelated patients with a characteristic phenotype associated with overlapping de novo deletions in the distal region of 17p13.1 detected with array comparative genomic hybridization and confirmed by real-time PCR. These patients share remarkably similar clinical features including microcephaly, mild developmental delay, generalized joint laxity, and a body posture with knee and elbow flexion and hands held in midline. They have distinctive facial features which include long midface with retrognathia with overbite, and protruding ears. The deletions in both patients are the smallest ever reported in this region (approximately 252 and 219 kb). The overlapping region contains 18 genes. Various isolated deletions of the 17p13.1 region have been reported previously without delineation of a consistent phenotype. We propose that the described microdeletions in the distal portion of 17p13.1 represent a novel microdeletion syndrome.


Asunto(s)
Cromosomas Humanos Par 17 , Facies , Eliminación de Gen , Discapacidad Intelectual/genética , Microcefalia/genética , Secuencia de Bases , Niño , Cartilla de ADN , Femenino , Humanos , Masculino , Fenotipo , Reacción en Cadena en Tiempo Real de la Polimerasa
10.
Exp Cell Res ; 317(11): 1513-26, 2011 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-21514294

RESUMEN

Glioblastoma multiforme (GBM) is the most common, and most aggressive primary brain tumor among adults. A vast majority of the tumors express high levels of the epidermal growth factor receptor (EGFR) as a consequence of gene amplification. Furthermore, gene amplification is often associated with mutation of EGFR, and the constitutive activated deletion variant EGFRvIII is the most common EGFR mutation found in GBM. Activated EGFR signaling, through overexpression and/or mutation, is involved in increased tumorigenic potential. As such, EGFR is an attractive target for GBM therapy. However, clinical studies with EGFR inhibitors have shown inconsistent results, and as such, further knowledge regarding the role of EGFR and EGFRvIII in GBM is needed. For this, an appropriate in vivo/in vitro tumor model is required. Here, we report the establishment of an experimental GBM model in which the expressions of EGFR and EGFRvIII are maintained both in xenograft tumors growing subcutaneously on mice and in cell cultures established in stem cell conditions. With this model it will be possible to further study the role of EGFR and EGFRvIII, and response to targeted therapy, in GBM.


Asunto(s)
Neoplasias Encefálicas/metabolismo , Receptores ErbB/metabolismo , Glioblastoma/metabolismo , Ensayos Antitumor por Modelo de Xenoinjerto , Animales , Western Blotting , Neoplasias Encefálicas/genética , Células Cultivadas , Endotelio Vascular/citología , Endotelio Vascular/metabolismo , Receptores ErbB/genética , Femenino , Fibroblastos/citología , Fibroblastos/metabolismo , Amplificación de Genes , Glioblastoma/genética , Humanos , Técnicas para Inmunoenzimas , Hibridación Fluorescente in Situ , Técnicas In Vitro , Pulmón/citología , Pulmón/metabolismo , Ratones , Ratones Desnudos , ARN Mensajero/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Esferoides Celulares/metabolismo , Células Madre/metabolismo
11.
Prenat Diagn ; 32(12): 1212-7, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23065819

RESUMEN

Submicroscopic terminal 6q deletions are rare. We report on two familial submicroscopic terminal 6q deletions ascertained because of prenatally detected isolated ventriculomegaly and further delineate the variable prenatal and postnatal phenotype. We review published cases of <5 Mb terminal 6q deletions.


Asunto(s)
Hidrocefalia/genética , Anomalías Múltiples/genética , Adulto , Deleción Cromosómica , Cromosomas Humanos Par 6/fisiología , Femenino , Humanos , Hidrocefalia/diagnóstico , Hidrocefalia/diagnóstico por imagen , Lactante , Recién Nacido , Cariotipificación , Masculino , Fenotipo , Embarazo , Ultrasonografía
12.
Artículo en Inglés | MEDLINE | ID: mdl-34117072

RESUMEN

The ETS2 repressor factor (ERF) is a transcription factor in the RAS-MEK-ERK signal transduction cascade that regulates cell proliferation and differentiation, and pathogenic sequence variants in the ERF gene cause variable craniosynostosis inherited in an autosomal dominant pattern. The reported ERF variants are largely loss-of-function, implying haploinsufficiency as a primary disease mechanism; however, ERF gene deletions have not been reported previously. Here we describe three probands with macrocephaly, craniofacial dysmorphology, and global developmental delay. Clinical genetic testing for fragile X and other relevant sequencing panels were negative; however, chromosomal microarray identified heterozygous deletions (63.7-583.2 kb) on Chromosome 19q13.2 in each proband that together included five genes associated with Mendelian diseases (ATP1A3, ERF, CIC, MEGF8, and LIPE). Parental testing indicated that the aberrations were apparently de novo in two of the probands and were inherited in the one proband with the smallest deletion. Deletion of ERF is consistent with the reported loss-of-function ERF variants, prompting clinical copy-number-variant classifications of likely pathogenic. Moreover, the recent characterization of heterozygous loss-of-function CIC sequence variants as a cause of intellectual disability and neurodevelopmental disorders inherited in an autosomal dominant pattern is also consistent with the developmental delays and intellectual disabilities identified among the two probands with CIC deletions. Taken together, this case series adds to the previously reported patients with ERF and/or CIC sequence variants and supports haploinsufficiency of both genes as a mechanism for a variable syndromic cranial phenotype with developmental delays and intellectual disability inherited in an autosomal dominant pattern.


Asunto(s)
Eliminación de Gen , Predisposición Genética a la Enfermedad/genética , Proteínas Represoras/genética , Cráneo/anomalías , Cráneo/crecimiento & desarrollo , Adolescente , Niño , Preescolar , Variaciones en el Número de Copia de ADN , Discapacidades del Desarrollo/genética , Femenino , Estudios de Asociación Genética , Pruebas Genéticas , Heterocigoto , Humanos , Discapacidad Intelectual/genética , Masculino , Proteínas de la Membrana/genética , Trastornos del Neurodesarrollo/genética , Fenotipo , Proteína Proto-Oncogénica c-ets-2/genética , Cráneo/patología , ATPasa Intercambiadora de Sodio-Potasio/genética , Factores de Transcripción/genética
13.
Am J Med Genet A ; 152A(3): 638-45, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20186789

RESUMEN

ZNF630 is a member of the primate-specific Xp11 zinc finger gene cluster that consists of six closely related genes, of which ZNF41, ZNF81, and ZNF674 have been shown to be involved in mental retardation. This suggests that mutations of ZNF630 might influence cognitive function. Here, we detected 12 ZNF630 deletions in a total of 1,562 male patients with mental retardation from Brazil, USA, Australia, and Europe. The breakpoints were analyzed in 10 families, and in all cases they were located within two segmental duplications that share more than 99% sequence identity, indicating that the deletions resulted from non-allelic homologous recombination. In 2,121 healthy male controls, 10 ZNF630 deletions were identified. In total, there was a 1.6-fold higher frequency of this deletion in males with mental retardation as compared to controls, but this increase was not statistically significant (P-value = 0.174). Conversely, a 1.9-fold lower frequency of ZNF630 duplications was observed in patients, which was not significant either (P-value = 0.163). These data do not show that ZNF630 deletions or duplications are associated with mental retardation.


Asunto(s)
Cromosomas Humanos X/genética , Eliminación de Gen , Discapacidad Intelectual/genética , Proteínas Represoras/genética , Estudios de Casos y Controles , Mapeo Cromosómico , Estudios de Cohortes , Hibridación Genómica Comparativa , Femenino , Dosificación de Gen , Duplicación de Gen , Humanos , Masculino , Discapacidad Intelectual Ligada al Cromosoma X/genética , Linaje , Fenotipo , Recombinación Genética
14.
Mol Syndromol ; 11(2): 83-89, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32655339

RESUMEN

Autosomal recessive omodysplasia (GPC6-related) is a rare short-limb skeletal dysplasia caused by biallelic mutations in the GPC6 gene. Affected individuals manifest with rhizomelic short stature, decreased mobility of elbow and knee joints as well as craniofacial anomalies. Both upper and lower limbs are severely affected. These manifestations contrast with normal height and limb shortening restricted to the arms in autosomal dominant omodysplasia (FZD2-related). Here, we report 2 affected brothers of Pakistani descent from Denmark with GPC6-related omodysplasia, aiming to highlight the clinical and radiological findings. A homozygous deletion of exon 6 in the GPC6 gene was detected. The pathognomonic radiological findings were distally tapered humeri and femora as well as severe proximal radioulnar diastasis. On close observations, we identified a recurrent and not previously described type of abnormal patterning in all long bones.

15.
Am J Med Genet A ; 149A(5): 894-905, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19363806

RESUMEN

Partial deletions of the long arm of chromosome 13 lead to variable phenotypes dependant on the size and position of the deleted region. In order to update the phenotypic map of chromosome 13q21.1-qter deletions, we applied 244k Agilent oligonucleotide-based array-CGH to determine the exact breakpoints in 14 patients with partial deletions of this region. Subsequently, we linked the genotype to the patient's phenotype. Using this approach, we were able to refine the smallest deletion region linked to short stature (13q31.3: 89.5-91.6 Mb), microcephaly (13q33.3-q34), cortical development malformations (13q33.1-qter), Dandy-Walker malformation (DWM) (13q32.2-q33.1), corpus callosum agenesis (CCA) (13q32.3-q33.1), meningocele/encephalocele (13q31.3-qter), DWM, CCA, and neural tube defects (NTDs) taken together (13q32.3-q33.1), ano-/microphthalmia (13q31.3-13qter), cleft lip/palate (13q31.3-13q33.1), lung hypoplasia (13q31.3-13q33.1), and thumb a-/hypoplasia (13q31.3-q33.1 and 13q33.3-q34). Based on observations of this study and previous reports we suggest a new entity, "distal limb anomalies association," linked to 13q31.3q33.1 segment. Most of the individuals with deletion of any part of 13q21qter showed surprisingly similar facial dysmorphic features, and thus, a "13q deletion facial appearance" was suggested. Prominent nasal columella was mapped between 13q31.3 and 13q33.3, and micrognathia between 13q21.33 and 13q31.1. The degree of mental delay did not display a particular phenotype-genotype correlation on chromosome 13. In contrast to previous reports of carriers of 13q32 band deletions as the most seriously affected patients, we present two such individuals with long-term survival, 28 and 2.5 years.


Asunto(s)
Deleción Cromosómica , Cromosomas Humanos Par 13/genética , Anomalías Congénitas/genética , Anomalías Congénitas/patología , Adolescente , Adulto , Niño , Preescolar , Mapeo Cromosómico , Anomalías Congénitas/clasificación , Femenino , Humanos , Lactante , Masculino , Análisis de Secuencia por Matrices de Oligonucleótidos , Fenotipo , Adulto Joven
16.
Folia Med (Plovdiv) ; 50(4): 55-62, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-19209531

RESUMEN

UNLABELLED: Cryptic chromosome aberrations are a common cause of idiopathic mental retardation and multiple congenital malformations syndromes (MR/MCM). MATERIAL AND METHODS: This study describes results and compares three methods for detection of submicroscopic chromosome aberrations in 76 children with MR/MCM and normal routine G-banded karyotype. RESULTS: Cryptic chromosome aberrations were detected in 15 patients (19.7%): in 3 of 19 patients (15.8%) by subtelomeric fluorescent in situ hybridization (FISH), in 5 of 47 patients (10.6%) by Multiplex Ligation Dependent Probe Amplification (MLPA) and in 7 of 23 patients (30.4%) by array-Comparative Genome Hybridization (array-CGH). Seven deletions, four duplications and four complex rearrangements have been diagnosed in the present study. Six were de novo and 2 were inherited from a parent carrier of balanced translocation. DISCUSSION: We observed a slightly higher imbalance incidence compared to the literature. Among these aberrations there were well known syndromes as well as some rare variants. CONCLUSION: This study confirms the utility of molecular-cytogenetic screening in patients with MR/MCM. We suggest array-CGH as the most reliable technique with a high diagnostic yield.


Asunto(s)
Anomalías Múltiples/genética , Aberraciones Cromosómicas , Discapacidad Intelectual/genética , Niño , Humanos , Discapacidad Intelectual/complicaciones , Técnicas de Diagnóstico Molecular
17.
Eur J Med Genet ; 61(8): 473-477, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29601900

RESUMEN

We report the clinical and neuroradiological findings in a young boy harboring the 9p deletion syndrome including the novel findings of thalamic infarction and germinal matrix haemorrhage and neonatal hyperinsulinemic hypoglycemia. Both the hypoglycemic events and the ventriculomegaly found in this patient have previously only been reported in two patients, while the thalamic infarction and germinal matrix haemorrhage are novel features.


Asunto(s)
Anomalías Múltiples/genética , Trastornos de los Cromosomas/genética , Hiperinsulinismo/genética , Hipoglucemia/genética , Anomalías Múltiples/patología , Deleción Cromosómica , Trastornos de los Cromosomas/patología , Cromosomas Humanos Par 9/genética , Humanos , Hiperinsulinismo/patología , Hipoglucemia/patología , Lactante , Masculino
18.
Nat Genet ; 50(10): 1442-1451, 2018 10.
Artículo en Inglés | MEDLINE | ID: mdl-30224647

RESUMEN

The etiological spectrum of ultra-rare developmental disorders remains to be fully defined. Chromatin regulatory mechanisms maintain cellular identity and function, where misregulation may lead to developmental defects. Here, we report pathogenic variations in MSL3, which encodes a member of the chromatin-associated male-specific lethal (MSL) complex responsible for bulk histone H4 lysine 16 acetylation (H4K16ac) in flies and mammals. These variants cause an X-linked syndrome affecting both sexes. Clinical features of the syndrome include global developmental delay, progressive gait disturbance, and recognizable facial dysmorphism. MSL3 mutations affect MSL complex assembly and activity, accompanied by a pronounced loss of H4K16ac levels in vivo. Patient-derived cells display global transcriptome alterations of pathways involved in morphogenesis and cell migration. Finally, we use histone deacetylase inhibitors to rebalance acetylation levels, alleviating some of the molecular and cellular phenotypes of patient cells. Taken together, we characterize a syndrome that allowed us to decipher the developmental importance of MSL3 in humans.


Asunto(s)
Enfermedades Genéticas Ligadas al Cromosoma X/genética , Histonas/metabolismo , Mutación , Trastornos del Neurodesarrollo/genética , Factores de Transcripción/genética , Acetilación , Adolescente , Animales , Estudios de Casos y Controles , Células Cultivadas , Niño , Preescolar , Proteínas Cromosómicas no Histona , Estudios de Cohortes , Proteínas de Unión al ADN , Femenino , Genes Ligados a X , Células HEK293 , Histona Acetiltransferasas/metabolismo , Humanos , Lactante , Masculino , Ratones , Ratones Transgénicos , Trastornos del Neurodesarrollo/metabolismo , Procesamiento Proteico-Postraduccional/genética , Síndrome
19.
Hum Mutat ; 28(7): 674-82, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17480035

RESUMEN

Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently, array-based comparative genomic hybridization (array CGH) has identified submicroscopic deletions and duplications as a common cause of MR, prompting us to search for such genomic imbalances in autism. Here we describe a 1.5-Mb duplication on chromosome 16p13.1 that was found by high-resolution array CGH in four severe autistic male patients from three unrelated families. The same duplication was identified in several variably affected and unaffected relatives. A deletion of the same interval was detected in three unrelated patients with MR and other clinical abnormalities. In one patient we revealed a further rearrangement of the 16p13 imbalance that was not present in his unaffected mother. Duplications and deletions of this 1.5-Mb interval have not been described as copy number variants in the Database of Genomic Variants and have not been identified in >600 individuals from other cohorts examined by high-resolution array CGH in our laboratory. Thus we conclude that these aberrations represent recurrent genomic imbalances which predispose to autism and/or MR.


Asunto(s)
Trastorno Autístico/genética , Cromosomas Humanos Par 16 , Duplicación de Gen , Predisposición Genética a la Enfermedad , Discapacidad Intelectual/genética , Hibridación de Ácido Nucleico/métodos , Niño , Preescolar , Bandeo Cromosómico , Estudios de Cohortes , Femenino , Humanos , Hibridación Fluorescente in Situ , Lactante , Masculino , Linaje , Reacción en Cadena de la Polimerasa
20.
Eur J Hum Genet ; 15(6): 711-3, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17392702

RESUMEN

Caspr2 is a member of neurexin superfamily, members of which are transmembrane proteins that mediate cellular interactions in the nervous system. Recently, truncation of the CNTNAP2 gene coding for the Caspr2 protein has been suggested to be associated with the Gilles de la Tourette syndrome, a neurological disorder characterized by motor and vocal tics, and behavioral anomalies. In this study, we describe a familial balanced reciprocal translocation t(7;15)(q35;q26.1) in phenotypically normal individuals. The 7q35 breakpoint disrupts the CNTNAP2 gene, indicating that truncation of this gene does not necessarily lead to the symptoms of the complex Gilles de la Tourette syndrome.


Asunto(s)
Cromosomas Humanos Par 15/genética , Cromosomas Humanos Par 7/genética , Proteínas de la Membrana/genética , Proteínas del Tejido Nervioso/genética , Translocación Genética/genética , Anomalías Múltiples/genética , Femenino , Humanos , Masculino , Linaje
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