Scapular winging
Autosomal RecessiveAutosomal DominantMitochondrialMuscular Dystrophy
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Overview
From WUSTL NeuromuscularMyopathies, Hereditary FSH Dystrophy: Often asymmetric LGMD 1F: TNPO3 1G: HNRNPDL 2A: Calpain 3 2D: α-Sarcoglycan 2E: β-Sarcoglycan 2I: FKRP 2N: POMT2 2S: TRAPPC11 2Z: POGLUT1 Emery-Dreifuss Myopathies ± Paget's disease of bone IBMPFD1: VCP IBMPFD2: HNRNPA2B1 MSP6: ANXA11 Desmin myopathy Early onset, Recessive Kaeser, Dominant Scapuloperoneal syndromes ACTA1 Centronuclear myopathy (MYF6): Adult-onset; Dominant Davidenkow's syndrome (SCPNK): Desmin FSH phenotype with ragged red fibers & cardiomyopathy Glycogen storage Acid maltase deficiency with scapuloperoneal weakness Phosphorylase deficienc
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Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.