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Differential Diagnosis For Psychomotor regression/infant/child

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Psychomotor regression/infant/child
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Metabolic, Storage Disorders: Pyruvate carboxylase enzyme deficiency/PCD; Hyperglycinemia, nonketotic; Sialidosis/Cherry Red Spot Myoclonus; Succinic Semialdehyde dehydrogenase Deficiency; Alpha-NAGA deficency (Schindler); Aspartylglycosaminuria; Fucosidosis (Anderson-Fabry); Gangliosidosis, generalized (GM1); Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia); Mucolipidosis IV (Bermans Syndrome)
Congenital, Developmental Disorders: Allan-Herndon Mental Retardation/X-linked; Alexander disease; Rett's syndrome; Landau-Kleffner Syndrome
Hereditary, Familial, Genetic Disorders: Infantile neuroaxonal dystrophy; Schilder disease/Adrenoleukodystrophy; Hereditary mitochondrial disorder; Pelizaeus-Merzbacher disease; Cerebellar ataxia/Cayman type
Synonyms: 0-11 years old, Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0-21), Impairment Psychomotor, Impairments Psychomotor, psychomotor impairment, Psychomotor Impairments, Regression
Definition: Be the first to add a definition for Psychomotor regression/infant/child
External Links Related to Psychomotor regression/infant/child: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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