Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
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Neonatal hypotonia and neuromuscular conditions
2019, Handbook of Clinical NeurologyCitation Excerpt :Progressive enlargement of the ventricles, however, is less frequent and only a minority will require shunt placement. This is a heterogeneous group of neuromuscular disorders characterized by weakness, usually from birth, or within 6 months, and dystrophic changes on muscle biopsy (Dubowitz, 1994; Philpot et al., 1995). Over the years the classification of CMD has become increasingly complicated due to the ever-growing numbers of genes and proteins identified (Muntoni and Voit, 2004; Mercuri and Longman, 2005; Godfrey et al., 2007).
Hypotonia and Weakness: Level of the Muscle
2018, Volpe's Neurology of the NewbornNeonatal Neuromuscular Disorders
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2017, Avery's Diseases of the Newborn, Tenth Edition
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