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Diagnostic approach to patients with a limb-girdle pattern of weakness and suspected muscular dystrophy with an autosomal recessive inheritance pattern.

Published byBasil Thornton Modified over 6 years ago

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Presentation on theme: "Diagnostic approach to patients with a limb-girdle pattern of weakness and suspected muscular dystrophy with an autosomal recessive inheritance pattern."— Presentation transcript:

1 Diagnostic approach to patients with a limb-girdle pattern of weakness and suspected muscular dystrophy with an autosomal recessive inheritance pattern. Autosomal dominant, autosomal recessive, or X-linked inheritance may be responsible in sporadic cases. LGMD, limb-girdle muscular dystrophy. (Reproduced with permission from Narayanaswami P, Weiss M, Selcen D, et al: Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine, Neurology. 2014;83(16):1453–1463.) Source: Muscular Dystrophies, Neuromuscular Disorders, 2e Citation: Amato AA, Russell JA. Neuromuscular Disorders, 2e; 2015 Available at: Accessed: November 03, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved

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