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Possible Causes For Neonatal Hypotonia/Floppy Baby Syndrome - Causes: Hereditary, Familial, Genetic Disorders

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Neonatal Hypotonia/Floppy Baby Syndrome - Causes
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Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes: Hereditary neuropathy; Muscular dystrophy; Muscular dystrophy, progressive; Spinal muscle atrophy; Spinal muscle atrophy, infantile; Chromosome 22q13.3 deletion syndrome (22q13.3); Juvenile spinal muscle atrophy (Kugelberg-Welander); Mitochondrial myopathy/MERRF; Beckwith-Wiedemann Syndrome; MELAS Encephalopathy; Dominant SCA/Spinal Cerebellar ataxias; Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3); Canavan disease; Central core disease; Cerebellar ataxia, congenital/hered.; Dysautonomia, familial; Leukodystrophy, Krabbe; Muscular atrophy, infantile, spinal; Myotonia congenita (Thomsens d.); Nemaline myopathy; Oculocerebrorenal dystrophy/Lowe syndrome; Oculopharyngeal muscular dystrophy; Progressive spinal muscular atrophy; Abducted thumbs syndrome; Congenital Muscular Dystrophy; Hereditary dysmyelinating neuropathy; Hereditary sensory neuropathy (type II); Myopathy, Desmin Storage type/Sarcoplasmin bodies; Myopathy, Myotubular/Centronuclear; Say Syndrome 1; Welander syndrome (See Kugelberg Welander)

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