Skip to main

Medical Subject Headings (thesaurus)

Search from vocabulary

mapear
anotar
descargar

Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle
Musculoskeletal Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle
... > Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle

Término preferido

Muscular Dystrophies, Limb-Girdle  

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

Tipo

  • mesh:Descriptor

Definición

  • A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).

Concepto genérico

Conceptos específicos

Conceptos relacionados

Etiquetas alternativas

  • Limb-Girdle Muscular Dystrophies
  • Limb-Girdle Muscular Dystrophy
  • Limb-Girdle Syndrome
  • Muscular Dystrophy, Limb-Girdle
  • Myopathic Limb-Girdle Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-S9ZFHT7J-F

Descargue este concepto:

RDF/XML TURTLE JSON-LD Creado 7/7/04, última modificación 8/7/13