Certain specified rare distal myopathy (Q85565): Difference between revisions

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Latest revision as of 10:55, 15 August 2026

Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive.

Language	Label	Description	Also known as
default for all languages	ID_1760014100
English	Certain specified rare distal myopathy	Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive.