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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Centronuclear (myotubular) myopathy

Figure 1

Male infant with X-linked centronuclear ("myotubular") myopathy due to a mutation in the myotubularin (MTM1) gene. Note generalised hypotonia and myopathic facial appearance with elongated face and inverted V-shaped mouth. (Reproduced from MedLink®Neurology, with permission)

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172