Ornithine carbamoyltransferase deficiency presenting with chorea in a female. | J Inherit Metab Dis;23(8): 843-4, 2000 Dec. | MEDLINE

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Ornithine carbamoyltransferase deficiency presenting with chorea in a female.

Wiltshire, E J; Poplawski, N K; Harbord, M G; Harrison, R J; Fletcher, J M.

Affiliation

Wiltshire EJ; Department of Chemical Pathology, Women's and Children's Hospital, North Adelaide, Australia

J Inherit Metab Dis ; 23(8): 843-4, 2000 Dec.

Article in En | MEDLINE | ID: mdl-11196111

Subject(s)

Chorea/enzymology; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid/urine; Alanine/blood; Chorea/blood; Chorea/urine; Female; Glutamine/blood; Humans; Infant; Uracil/urine

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Collection: 01-internacional Database: MEDLINE Main subject: Orotic Acid / Chorea / Ornithine Carbamoyltransferase Deficiency Disease Limits: Female / Humans / Infant Language: En Journal: J Inherit Metab Dis Year: 2000 Document type: Article Affiliation country: Australia

Search on Google

Collection: 01-internacional Database: MEDLINE Main subject: Orotic Acid / Chorea / Ornithine Carbamoyltransferase Deficiency Disease Limits: Female / Humans / Infant Language: En Journal: J Inherit Metab Dis Year: 2000 Document type: Article Affiliation country: Australia