Limb-girdle muscular dystrophy type 2H: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the TRIM32 protein. More detailed information about the symptoms, causes, and treatments of Limb-girdle muscular dystrophy type 2H is available below.
See full list of 6 symptoms of Limb-girdle muscular dystrophy type 2H
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Prognosis for Limb-girdle muscular dystrophy type 2H: slow progression with wheelchair confinement usually in 4th decade or later
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Limb-girdle muscular dystrophy type 2H is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Limb-girdle muscular dystrophy type 2H, or a subtype of Limb-girdle muscular dystrophy type 2H,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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