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LGMD2H (medical condition): An autosomal recessive form of limb-girdle muscular dystrophy...more »
LGMD2H is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that LGMD2H, or a subtype of LGMD2H,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
LGMD2H: Another name for Limb-girdle muscular dystrophy type 2H (or close medical condition association).
»Introduction: Limb-girdle muscular dystrophy type 2H
»Symptoms of Limb-girdle muscular dystrophy type 2H
LGMD2H: LGMD2H is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of LGMD2H incude:
These medical disease topics may be related to LGMD2H:
Source - NIH
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