Hartnup disease

Indian Journal of Dermatology

Volumn 53, Issue 1, 2008, Pages 31-32

  Patel, A ^a,b   Prabhu, A ^a  

^a GOVERNMENT MEDICAL COLLEGE   (India)

^b NONE   (India)

Author keywords

Hartnup disease; Pellagra; Tryptophan

Indexed keywords

ALPHA AMINO ACID; AMINO ACID TRANSPORTER; NICOTINIC ACID; TRYPTOPHAN;

AMINOACIDURIA; ARTICLE; ATAXIA; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DIARRHEA; FEMALE; HARTNUP DISEASE; HUMAN; KIDNEY TUBULE; MENTAL DISEASE; NICOTINIC ACID DEFICIENCY; RASH; SCHOOL CHILD; SMALL INTESTINE ABSORPTION; URINALYSIS;

EID: 42549110399     PISSN: 00195154     EISSN: 19983611     Source Type: Journal    
DOI: 10.4103/0019-5154.39740     Document Type: Article

References (2)

1. Baron DN, Dent CE, Harris H, Hart EW, Jepson JB. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria and other bizarre biochemical features. Lancet 1956;271:421-8.
2. Nozaki J, Dakeishi M, Ohura T, Inoune K, Manabe M, Wada Y, et al. Homozygosity mapping to chromosome 5 p 15 of a gene responsible for Hartnup Disorder. Biochem Biophys Res Commun 2001;284:255-60.