Key result
Dysferlinopathies are rare autosomal recessive neuromuscular diseases that can account for up to 30% of progressive recessive muscular dystrophies in the Middle East and Indian subcontinent.
Population
Patients with dysferlinopathies
Design
Review
Authors
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May inform regional diagnostic strategies for muscular dystrophies; leaves open larger prevalence studies across diverse populations.
Dysferlinopathies are a diverse group of autosomal recessive neuromuscular diseases that may benefit from innovative therapies targeting membrane repair and vesicle trafficking.
Urtizberea et al. (2008) conducted a review in Dysferlinopathies. Dysferlinopathies are rare autosomal recessive neuromuscular diseases that can account for up to 30% of progressive recessive muscular dystrophies in the Middle East and Indian subcontinent.
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