Recessive limb-girdle muscular dystrophy (Q41384): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Distrofias musculares de cinturas autossômicas recessivas (DMC2) são um grupo de doenças geneticamente heterogêneas que são tipicamente caracterizadas por fraqueza progressiva e atrofia dos músculos do ombro e da cintura pélvica. Muitas das mais de 20 condições diferentes apresentam características clínicas sobrepostas com outras formas de distrofia muscular, miopatias congênitas, miofibrilares ou mesmo distais e também com doenças musculares adquiridas. Embora individualmente extremamente raros, todos os tipos de DMC2 juntos formam um importante grupo de diagnóstico diferencial entre as doenças neuromusculares.
@@ description / en / description / en @@
+Autosomal recessive limb girdle muscular dystrophies (LGMD2) are a group of genetically heterogeneous diseases that are typically characterised by progressive weakness and wasting of the shoulder and pelvic girdle muscles. Many of the more than 20 different conditions show overlapping clinical features with other forms of muscular dystrophy, congenital, myofibrillar or even distal myopathies and also with acquired muscle diseases. Although individually extremely rare, all types of LGMD2 together form an important differential diagnostic group among neuromuscular diseases.
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+CID11:8C70.41
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-13T00:00:00Z
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+G71.0
@@ Property / Linked ICD 10: G71.0 / rank @@
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Latest revision as of 07:32, 13 August 2026

Autosomal recessive limb girdle muscular dystrophies (LGMD2) are a group of genetically heterogeneous diseases that are typically characterised by progressive weakness and wasting of the shoulder and pelvic girdle muscles. Many of the more than 20 different conditions show overlapping clinical features with other forms of muscular dystrophy, congenital, myofibrillar or even distal myopathies and also with acquired muscle diseases. Although individually extremely rare, all types of LGMD2 together form an important differential diagnostic group among neuromuscular diseases.

Language	Label	Description	Also known as
default for all languages	8C70.41
English	Recessive limb-girdle muscular dystrophy	Autosomal recessive limb girdle muscular dystrophies (LGMD2) are a group of genetically heterogeneous diseases that are typically characterised by progressive weakness and wasting of the shoulder and pelvic girdle muscles. Many of the more than 20 different conditions show overlapping clinical features with other forms of muscular dystrophy, congenital, myofibrillar or even distal myopathies and also with acquired muscle diseases. Although individually extremely rare, all types of LGMD2 together form an important differential diagnostic group among neuromuscular diseases.