Dominant limb-girdle muscular dystrophy (Q41383): Difference between revisions

@@ description / pt-br / description / pt-br @@
+As distrofias musculares de cinturas (DMC) são um grupo de doenças genéticas caracterizadas predominantemente por atrofia e fraqueza progressiva dos músculos da cintura proximal do membro, incluindo os músculos pélvicos, do ombro, do braço e da coxa. Os sintomas iniciais geralmente variam desde a primeira infância até o final da idade adulta, e a velocidade de progressão e distribuição de fraqueza e debilidade também variam consideravelmente entre os indivíduos e subtipos genéticos. Existem atualmente 8 DMC autossômicos dominantes (DMC1), ligados a mutações genéticas específicas. As DMC dominantes são frequentemente alélicas com outros transtornos clínicos, incluindo as miopatias miofibrilares ou cardiomiopatia dilatada.
@@ description / en / description / en @@
+The Limb Girdle Muscular Dystrophies (LGMD) are a group of genetic disorders characterised predominantly by progressive wasting and weakness of proximal limb girdle muscles, including pelvic, shoulder, upper arm and thigh muscles. The onset symptoms usually vary from early childhood to late adulthood, and the progression rate and distribution of weakness and wasting also varies considerably among individuals and genetic subtypes. There are currently 8 autosomal dominant LGMDs (LGMD1), linked to specific gene mutations. Dominant LGMDs are often allelic with other clinical disorders, including the myofibrillar myopathies or dilated cardiomyopathy.
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+CID11:8C70.40
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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
-Timezone
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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

The Limb Girdle Muscular Dystrophies (LGMD) are a group of genetic disorders characterised predominantly by progressive wasting and weakness of proximal limb girdle muscles, including pelvic, shoulder, upper arm and thigh muscles. The onset symptoms usually vary from early childhood to late adulthood, and the progression rate and distribution of weakness and wasting also varies considerably among individuals and genetic subtypes. There are currently 8 autosomal dominant LGMDs (LGMD1), linked to specific gene mutations. Dominant LGMDs are often allelic with other clinical disorders, including the myofibrillar myopathies or dilated cardiomyopathy.

Language	Label	Description	Also known as
default for all languages	8C70.40
English	Dominant limb-girdle muscular dystrophy	The Limb Girdle Muscular Dystrophies (LGMD) are a group of genetic disorders characterised predominantly by progressive wasting and weakness of proximal limb girdle muscles, including pelvic, shoulder, upper arm and thigh muscles. The onset symptoms usually vary from early childhood to late adulthood, and the progression rate and distribution of weakness and wasting also varies considerably among individuals and genetic subtypes. There are currently 8 autosomal dominant LGMDs (LGMD1), linked to specific gene mutations. Dominant LGMDs are often allelic with other clinical disorders, including the myofibrillar myopathies or dilated cardiomyopathy.