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Differential Diagnosis For Limb Ataxia

List of current finding(s):

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: Paraneoplastic syndrome; Cerebellar/vermis lesion; Cerebellum hemangioblastoma; Neuroblastoma; Posterior fossa tumor/lesion; Carcinoma, bronchogenic; Cerebellar tumor; Cerebellopontine angle tumor
Allergic, Collagen, Auto-Immune Disorders: Acute Postinfectious Cerebellitis
Metabolic, Storage Disorders: Glucose 6 PD deficiency; Porphyria, acute intermittent; Hydroxyprolinemia, congenital; Carnitine/Acylcarnitine translocase deficiency; Citrullinemia/Argininsuccinicaciduria; Combined carboxylase/Biotinidase deficiency; HyperArgininemia; Ketothiolase deficiency; Ketotic hyperglycinemia, idiopathic; Methylmalonic acidemia/ketotic glycine; Phenylketonuria/PKU; Propionicacidemia/ketotic glycinemia; Pyroglutamic acidemia; Pyruvate carboxylase enzyme deficiency/PCD; 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; Hartnup disease; Histidinemia; Homocystinuria/homocystinemia; Hyperprolinemia; Maple syrup urine 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: Joubert syndrome/absent cerebellar vermis (unco); Dandy-Walker anomaly/syndrome; Happy puppet syndrome/Angelman syndrome; Machado-Joseph Syndrome; Prader-Willi syndrome
Hereditary, Familial, Genetic Disorders: Ataxia-telangiectasia; Cerebellar hereditofamilial degen.; Juvenile spinal muscle atrophy (Kugelberg-Welander); Dominant SCA/Spinal Cerebellar ataxias; Cerebellar ataxia, congenital/hered.; Encephalomyelopathy/necro/subact/Leigh; Friedreich's Ataxia; Hereditary mitochondrial disorder; Olivopontocerebellar degeneration; Pelizaeus-Merzbacher disease; Welander syndrome (See Kugelberg Welander)
Usage, Degenerative, Necrosis, Age Related Disorders: Cerebellum degeneration, cortical par.; Cerebellar degeneration, subacute; Gerstmann-Straussler-Scheinker (GSS) Disease
Relational, Mental, Psychiatric Disorders: Development impairment, childhood
Anatomic, Foreign Body, Structural Disorders: Cerebellar mass lesion
Arteriosclerotic, Vascular, Venous Disorders: Cerebellar hemorrhage/hematoma; Cerebellar infarct; Anterior Cerebral Artery Thrombosis
Reference to Organ System: Cerebellar syndrome, acquired
Drugs: Phenothiazine dystonic/toxicity
Poisoning (Specific Agent): Alcohol/Ethanol ingestion/intake; Lead poisoning in children; Alcoholic cerebellar degeneration; Mercury salts/bichloride acute toxicity; Mercury poisoning/infant/child
Synonyms: Ataxia, Ataxia (D), Ataxia (D) (finding), Ataxia (finding), Ataxia unspecified, Ataxias, Ataxy, Coordination Impairment, Coordination Impairments, Dyssynergia, Impairment Coordination, Impairments Coordination, Limb
Definition: Be the first to add a definition for Limb Ataxia
External Links Related to Limb Ataxia: 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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