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Differential Diagnosis For Limb ataxia/clumsiness child

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Limb ataxia/clumsiness child
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Electromagnetic, Physics, trauma, Radiation Causes: Hypoxia; Hypoxic environment; Hypothermia, accidental/exposure; High altitude cerebral edema
Infectious Disorders (Specific Agent): Encephalitis, Dawsons/inclusion body
Neoplastic Disorders: Cerebellar tumor
Allergic, Collagen, Auto-Immune Disorders: Acute Postinfectious Cerebellitis
Metabolic, Storage Disorders: Glucose 6 PD deficiency; Abetalipoproteinemia (Bassen Kornzweig); Hydroxyprolinemia, congenital; Carnitine/Acylcarnitine translocase deficiency; Citrullinemia/Argininsuccinicaciduria; Combined carboxylase/Biotinidase deficiency; French-Canadian type COX mitochondrial defect; HyperArgininemia; Ketothiolase deficiency; Ketotic hyperglycinemia, idiopathic; Methylmalonic acidemia/ketotic glycine; Mitochondrial respiratory chain defects; Phenylketonuria/PKU; Propionicacidemia/ketotic glycinemia; Pyroglutamic acidemia; Pyruvate carboxylase enzyme deficiency/PCD; Infantile mitochondrial myopathy/Cox defect; Aminoacid enzyme/metabolic disorder; Beta-hydroxyisolvaleric acidemia; Glutamic acidemia; Krebs cycle/EM cycle metabolic disorder; Lysinemia; Prolinemia/type II; Proprionic acidemia/congenital; Succinic Semialdehyde dehydrogenase Deficiency; Tyrosinemia, hereditary; Valinemia/Hypervalinemia; Wilsons Disease; Carnitine palmityltranferase deficiency; Cystathioninuria; Fructose 1,6 diphosphatase deficiency; Histidinemia; Homocystinuria/homocystinemia; Hyperprolinemia; Maple syrup urine disease; Sandhoff disease; Sarcosinemia; Organic acidemias/Metabolic syndromes
Biochemical Disorders: Hypoxia, systemic, chronic; Hypoglycemia
Deficiency Disorders: Vitamin E defic. in newborns; Vitamin E deficiency
Congenital, Developmental Disorders: Asperger syndrome (mild autism); Happy puppet syndrome/Angelman syndrome; Cerebral gigantism of childhood (Sotos); Prader-Willi syndrome
Hereditary, Familial, Genetic Disorders: Juvenile spinal muscle atrophy (Kugelberg-Welander); Mitochondrial myopathy/MERRF; Dominant SCA/Spinal Cerebellar ataxias; Cerebellar ataxia, congenital/hered.; Encephalomyelopathy/necro/subact/Leigh; Hereditary mitochondrial disorder; Pelizaeus-Merzbacher disease; Welander syndrome (See Kugelberg Welander)
Usage, Degenerative, Necrosis, Age Related Disorders: Primary lateral sclerosis
Relational, Mental, Psychiatric Disorders: Development impairment, childhood
Drugs: Phenothiazine dystonic/toxicity
Poisoning (Specific Agent): Alcohol/Ethanol ingestion/intake; Lead poisoning in children; Mercury salts/bichloride acute toxicity; Mercury poisoning/infant/child
Synonyms: 0-11 years old, Ataxia, Ataxia (D), Ataxia (D) (finding), Ataxia (finding), Ataxia unspecified, Ataxias, Ataxy, Awkwardness, Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0-21), clumsiness, Clumsiness (finding), clumsiness syndrome, Coordination Impairment, Coordination Impairments, Dyssynergia, Impairment Coordination, Impairments Coordination, syndrome clumsiness
Definition: Be the first to add a definition for Limb ataxia/clumsiness child
External Links Related to Limb ataxia/clumsiness 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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