RESUMEN
OBJECTIVE: To expand the clinical and genetic spectrum of nemaline myopathy 10 by a series of Austrian and German patients with a milder disease course and missense mutations in LMOD3. METHODS: We characterized the clinical features and the genetic status of 4 unrelated adolescent or adult patients with nemaline myopathy. RESULTS: The 4 patients showed a relatively mild disease course. They all have survived into adulthood, 3 of 4 have remained ambulatory, and all showed marked facial weakness. Muscle biopsy specimens gave evidence of nemaline bodies. All patients were unrelated but originated from Austria (Tyrol and Upper Austria) and Southern Germany (Bavaria). All patients carried the missense variant c.1648C>T, p.(Leu550Phe) in the LMOD3 gene, either on both alleles or in trans with another missense variant (c.1004A>G, p.Gln335Arg). Both variants were not reported previously. CONCLUSIONS: In 2014, a severe form of congenital nemaline myopathy caused by disrupting mutations in LMOD3 was identified and denoted as NEM10. Unlike the previously reported patients, who had a severe clinical picture with a substantial risk of early death, our patients showed a relatively mild disease course. As the missense variant c.1648C>T is located further downstream compared to all previously published LMOD3 mutations, it might be associated with higher protein expression compared to the reported loss-of-function mutations. The apparent clusters of 2 mild mutations in Germany and Austria in 4 unrelated families may be explained by a founder effect.
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Proteínas Musculares/genética , Miopatías Nemalínicas/genética , Adolescente , Adulto , Austria , Femenino , Alemania , Humanos , Masculino , Proteínas de Microfilamentos , Mutación Missense , FenotipoRESUMEN
We describe a 7-year-old girl who presented with loss of appetite, weakness and excercise intolerance. Enzyme investigation of the respiratory chain in muscle tissue revealed a combined complex I, III and IV deficiency. A novel heteroplasmic G-->A exchange at nucleotide position 14739 was found in the MTTE gene of the tRNA glutamic acid. The mutation load in muscle was 72%, urine sediment 38%, blood 31% and fibroblasts 29% and it correlated with COX-negative fibres. Our patient presented with a predominantly myopathic phenotype. The G14739A mutation is the third reported in the mitochondrial tRNA glutamic acid gene, and it occurred in a sporadic case.
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Enfermedades Mitocondriales/genética , Miopatías Mitocondriales/genética , Músculo Esquelético/metabolismo , Mutación/genética , ARN de Transferencia/genética , ARN/genética , Encéfalo/patología , Niño , Análisis Mutacional de ADN , Tolerancia al Ejercicio/genética , Femenino , Predisposición Genética a la Enfermedad/genética , Ácido Glutámico/metabolismo , Humanos , Enfermedades Mitocondriales/metabolismo , Enfermedades Mitocondriales/fisiopatología , Miopatías Mitocondriales/metabolismo , Miopatías Mitocondriales/fisiopatología , Fibras Musculares Esqueléticas/metabolismo , Fibras Musculares Esqueléticas/patología , Debilidad Muscular/genética , Debilidad Muscular/metabolismo , Debilidad Muscular/fisiopatología , Músculo Esquelético/patología , Músculo Esquelético/fisiopatología , ARN MitocondrialRESUMEN
BACKGROUND: Kindler syndrome (online Mendelian Inheritance in Man No. 173650) is an autosomal recessive genodermatosis characterized by acral trauma-induced blistering that improves with age and by progressive poikiloderma in later life. Other clinical features include photosensitivity, webbing of the fingers and toes, nail dystrophy, periodontal disease, and mucosal alterations. Aside from esophageal or anal stenosis, gastrointestinal tract involvement seems to be rare in Kindler syndrome. Recently, mutations in the KIND1 gene that encodes for the membrane-associated protein kindlin-1 have been identified. Kindlin-1 links the actin cytoskeleton to the extracellular matrix and is supposed to have cell-signaling functions owing to different functional domains. In particular, a domain with high homology to 4.1/ezrin/radixin/moesin (FERM) proteins is closely related to the sequences of talin that mediate integrin binding and therefore may play a role in integrin-dependent processes such as cell growth, differentiation, and apoptosis. OBSERVATION: Complete loss of this multifunctional protein in our patient with Kindler syndrome resulted in severe gastrointestinal tract involvement with hemorrhagic colitis. Mucosa of the descending and sigmoid colon and the rectum showed erosions and ulcers with pseudomembranous alterations of an overall highly vulnerable mucosa. Mutation analysis revealed a homozygous status for the novel mutation 20/21delTT in exon 2 of the KIND1 gene resulting in a preterminal stop codon creating a nonfunctional peptide 17 amino acids in length. CONCLUSION: Because of our experience with this and another patient, we propose that gastrointestinal tract involvement should be looked at more frequently in Kindler syndrome.
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Colitis Ulcerosa/genética , ADN/genética , Epidermólisis Ampollosa Distrófica/genética , Proteínas de la Membrana/genética , Mutación , Proteínas de Neoplasias/genética , Adulto , Biopsia , Colitis Ulcerosa/complicaciones , Colitis Ulcerosa/patología , Colonoscopía , Progresión de la Enfermedad , Epidermólisis Ampollosa Distrófica/complicaciones , Epidermólisis Ampollosa Distrófica/patología , Femenino , Predisposición Genética a la Enfermedad , Haplotipos , Humanos , Recién Nacido , Masculino , Microscopía Electrónica de Transmisión , Pronóstico , Piel/ultraestructura , SíndromeRESUMEN
PURPOSE: To describe the histopathologic changes in the cornea following amniotic membrane transplantation (AMT) combined with limbal transplantation. METHODS: Four eyes with complete limbal stem cell deficiency after severe chemical burn underwent AMT with either a living-related conjunctival limbal allograft (lr-CLAL) (three eyes) or a conjunctival limbal autograft (CLAU) (one eye) for ocular surface reconstruction. Penetrating keratoplasty was performed several months after the initial procedure for further visual rehabilitation. Mean follow up time was 20 months. Light and transmission electron microscopy (TEM) and indirect immunofluorescence microscopy of the excised corneal buttons were performed. RESULTS: All specimens displayed a multilayered epithelium without conjunctival goblet cells over the entire corneal surface. Basal epithelial cells demonstrated a firm connection to the remnants of the transplanted amniotic membrane (AM), which at some places appeared to be in a state of "modification" or "remodeling" in the collagen layers. The basement membrane zone displayed a positive staining when using antibodies against collagen IV and VII, integrin alpha6 and beta4, laminin 5, and bullous pemphigoid antigen 2. Remnants of the AM in the specimen showed staining of collagen IV, which was found also in cross-sections of cryopreserved AM. The recipients Bowman's membranes that were only partially present after the initial trauma were significantly disturbed. CONCLUSION: Within the time frame studied, the transplanted AM apparently survives and integrates into the host tissue being modified or remodeled by recipient cells. AMT in combination with a CLAU or lr-CLAL is a useful technique in promoting a rapid and stable reepithelialization of a corneal surface following severe chemical or thermal damage.
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Amnios/trasplante , Quemaduras Químicas/patología , Conjuntiva/citología , Córnea/patología , Células Epiteliales/trasplante , Quemaduras Oculares/inducido químicamente , Trasplante de Células Madre , Adolescente , Adulto , Biomarcadores/análisis , Quemaduras Químicas/metabolismo , Quemaduras Químicas/cirugía , Trasplante de Células , Terapia Combinada , Conjuntiva/metabolismo , Conjuntiva/ultraestructura , Córnea/metabolismo , Células Epiteliales/metabolismo , Células Epiteliales/ultraestructura , Proteínas de la Matriz Extracelular/metabolismo , Quemaduras Oculares/metabolismo , Quemaduras Oculares/patología , Técnica del Anticuerpo Fluorescente Indirecta , Humanos , Queratoplastia Penetrante , Masculino , Microscopía Fluorescente , Persona de Mediana Edad , Células Madre/metabolismo , Células Madre/ultraestructuraRESUMEN
Functional defects in type VII collagen, caused by premature termination codons on both alleles of the COL7A1 gene, are responsible for the severe autosomal recessive types of the skin blistering disease, recessive dystrophic epidermolysis bullosa (RDEB). The full-length COL7A1 complementary DNA (cDNA) is about 9 kb, a size that is hardly accommodated by therapeutically used retroviral vectors. Although there have been successful attempts to produce functional type VII collagen protein in model systems of RDEB, the risk of genetic rearrangements of the large repetitive cDNA sequence may hamper the clinical application of full-length COL7A1 cDNA in the human system. Therefore, we used trans-splicing to reduce the size of the COL7A1 transcript. Retroviral transduction of RDEB keratinocytes with a 3' pre-trans-splicing molecule resulted in correction of full-length type VII collagen expression. Unlike parental RDEB keratinocytes, transduced cells displayed normal morphology and reduced invasive capacity. Moreover, transduced cells showed normal localization of type VII collagen at the basement membrane zone in skin equivalents, where it assembled into anchoring fibril-like structures. Thus, using trans-splicing we achieved correction of an RDEB phenotype in vitro, which marks an important step toward its application in gene therapy in vivo.
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Codón sin Sentido/genética , Colágeno Tipo VII/genética , Epidermólisis Ampollosa Distrófica , Terapia Genética/métodos , Transducción Genética/métodos , Empalme Alternativo/genética , Biopsia , Células Cultivadas , Epidermólisis Ampollosa Distrófica/genética , Epidermólisis Ampollosa Distrófica/patología , Epidermólisis Ampollosa Distrófica/terapia , Humanos , Queratinocitos/patología , Queratinocitos/fisiología , Técnicas de Cultivo de Órganos , Fenotipo , ARN Mensajero/genética , Retroviridae/genéticaRESUMEN
During early odontogenesis the basement membrane is known to be important in epithelio-mesenchymal interactions. Mutations in the gene of one of the major structural proteins of the basement membrane such as laminin 5 might therefore be expected either to seriously compromise ameloblast differentiation and/ or interfere with normal basement-membrane formation and degradation and thus the binding of the ameloblasts to their underlying matrix. Teeth of patients suffering from junctional epidermolysis bullosa (JEB) can be severely affected by abnormal dental development and generalized or focal enamel hypoplasia. Those changes are found in 100% of individuals with JEB but the expression is variable. Beside the quantitative alterations, changes in the prismatic structure and orientation of enamel crystals are described. In addition JEB is associated with an increased risk for dental caries, caused by developmentally compromised enamel and external factors such as difficulties in maintaining oral hygiene because of oral lesions or a softer and more refined high caloric diet. Dental care includes three main strategies: Prevention by consequent oral hygiene and reduction of cariogenic nutrition is of paramount importance to minimize caries development; the restoration of enamel and dentin defects with fillings and stainless steel crowns to guarantee structure and function of teeth; and extractions of most severely affected teeth with osteolytic foci to remove continuous sources of oral infections.
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Moléculas de Adhesión Celular/genética , Epidermólisis Ampollosa de la Unión/complicaciones , Epidermólisis Ampollosa de la Unión/genética , Anomalías Dentarias/etiología , Adulto , Atención Odontológica , Caries Dental/etiología , Caries Dental/prevención & control , Susceptibilidad a Caries Dentarias , Hipoplasia del Esmalte Dental/diagnóstico , Hipoplasia del Esmalte Dental/etiología , Epidermólisis Ampollosa de la Unión/diagnóstico , Femenino , Humanos , Mutación , Radiografía Panorámica , Factores de Riesgo , Anomalías Dentarias/diagnóstico , Anomalías Dentarias/diagnóstico por imagen , KalininaRESUMEN
We report the case of a 56-year-old female patient who presented with an inflamed, ulcerated lesion on the left side of her neck after contact (scratch) with a cat living in the patient's house. Satellite lesions developed despite local treatment and parenteral clindamycin. Histopatholgic examination and the Tzanck test showed evidence of a viral infection. Subsequent transmission electron microscopy of scrap tissue and material from a fresh pustule exhibited multiple typical poxvirus particles, predominantly in remnants of scaled-off layers of degenerated keratinocytes, and virus particles in intermingled phagocytes, leading to the diagnosis of feline Orthopoxvirus (cowpox virus) infection. These results were verified by polymerase chain reaction and sequencing. Concern has been raised as to whether discontinuation of smallpox vaccine would cause an increase in Orthopoxvirus infection, but this has not yet shown to be the case.