Nemaline Rod Myopathy
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"Nemaline rod myopathy is an inherited congenital myopathy first described in 1963. Affected patients characteristically present in infancy with a non-progressive hypotonia and symmetrical muscle weakness. The disease affects all skeletal muscles including the diaphragm with sparing of cardiac and other muscle. Facial dysmorphism is common as are skeletal deformities, including kyphosis, scolosis and pectus excavatum."
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scoliosis, bulbar palsy-cranial-nerve-9-12, kyphosis, pectus excavatum

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Anaesthetic implications of nemaline rod myopathy. Review
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