2,8-dihydroxyadenine urolithiasis, an underdiagnosed disease

The Lancet

Volumn 339, Issue 8800, 1992, Pages 1050-1051

  Ceballos Picot, I ^a   Perignon, J L ^a   Hamet, M ^a   Daudon, M ^b   Kamoun, P ^b  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b Laboratory of Biochemistry A Crystal Laboratory Hôpital Necker Enfants Malades ^*  (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

2,8 DIHYDROXYADENINE; ALLOPURINOL;

ADULT; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME DEFICIENCY; FRANCE; HUMAN; LETTER; PRIORITY JOURNAL; UROLITHIASIS;

ADENINE; ADENINE PHOSPHORIBOSYLTRANSFERASE; ADULT; AGED; CHILD; FEMALE; HUMAN; MALE; MIDDLE AGE; URINARY CALCULI;

EID: 0026576093     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/0140-6736(92)90569-O     Document Type: Letter

References (5)

1. Adenine phosphonbosyltransferase: a simple spectrophotometric assay and the incidence of mutation in the normal population
2. 2,8-dihydroxyadenine lithiasis
3. Adenine phosphoribosyltransferase deficiency and 2,8-dihydroxyadenine lithiasis
4. Une nouvelle maladie metabolique: le deficit complet en adenine phosphoribosyltransferase avec lithiase de 2,8-dihydroxyadenine
5. Epidemiologie de la lithiase urinaire dans la région de Saint-Brieuc. Etude prospective sur 4 ans (1986-1989)