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1.
Neuromuscul Disord ; 10(4-5): 240-6, 2000 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10838249

RESUMEN

Autosomal recessive limb-girdle muscular dystrophies represent a genetically heterogeneous group of diseases characterized by a progressive involvement of skeletal muscles. They show a wide spectrum of clinical courses, varying from very mild to severe. Eight loci responsible for autosomal recessive limb-girdle muscular dystrophies have been mapped and six defective genes identified. In this study, we report the clinical data, muscle biopsy findings and results of genetic linkage analysis in a large consanguineous Tunisian family with 13 individuals suffering from autosomal recessive limb-girdle muscular dystrophy. Clinical features include variable age of onset, proximal limb muscle weakness and wasting predominantly affecting the pelvic girdle, and variable course between siblings. CK rate was usually high in younger patients. Muscle biopsy showed dystrophic changes with normal expression of dystrophin and various proteins of the dystrophin-associated protein complex (sarcoglycan sub-units, dystroglycan, and sarcospan). Genetic linkage analysis excluded the known limb-girdle muscular dystrophies loci as well as ten additional candidate genes. A maximum LOD score of 4.36 at θ=0.00 was obtained with marker D19S606, mapping this new form of autosomal recessive limb-girdle muscular dystrophy to chromosome 19q13.3.


Asunto(s)
Cromosomas Humanos Par 19/genética , Distrofias Musculares/genética , Adolescente , Adulto , Mapeo Cromosómico , Consanguinidad , Femenino , Genes Recesivos/genética , Humanos , Escala de Lod , Masculino , Persona de Mediana Edad , Músculo Esquelético/patología , Distrofias Musculares/patología , Linaje , Túnez
2.
Neurology ; 60(8): 1341-4, 2003 Apr 22.
Artículo en Inglés | MEDLINE | ID: mdl-12707439

RESUMEN

The authors mapped an autosomal recessive form of limb-girdle MD on chromosome 19q13.3 (LGMD2I), further narrowed down the candidate region to 1.1 Mb, and identified one new homozygous mutation in the fukutin-related protein (FKRP) gene on patients of the original Tunisian family. Immunohistochemical and immunoblot analysis showed abnormal expression of alpha-dystroglycan and laminin-alpha2 supporting the hypothesis that FKRP has a role in the interaction between the extracellular matrix components.


Asunto(s)
Distrofias Musculares/genética , Sustitución de Aminoácidos , Cromosomas Humanos Par 19/genética , Consanguinidad , Proteínas del Citoesqueleto/metabolismo , Distroglicanos , Genes Recesivos , Glicosilación , Humanos , Laminina/deficiencia , Laminina/metabolismo , Glicoproteínas de Membrana/metabolismo , Músculo Esquelético/química , Músculo Esquelético/patología , Distrofias Musculares/sangre , Distrofias Musculares/patología , Mutación Missense , Proteínas del Tejido Nervioso/genética , Pentosiltransferasa , Mutación Puntual , Procesamiento Proteico-Postraduccional , Proteínas , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Túnez
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