Alcaptonuria: A rare cause of abnormal coloration of the urine: A case report in the neonate;Lଁalcaptonurie: Une cause rare de coloration anormale des urines. À propos dଁun cas chez le nourrisson

Archives de Pediatrie

Volumn 7, Issue 8, 2000, Pages 844-846

  Adonis Koffy, L ^a   Gonzalees E ^a   Nathanson, S ^a   Spodek, C ^a   Bensman, A ^a  

^a ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

Alkaptonuria; Homogentisic acid

Indexed keywords

ALKYLATING AGENT; ASCORBIC ACID; HOMOGENTISIC ACID;

ALKAPTONURIA; ARTICLE; CASE REPORT; CHROMATOGRAPHY; EARLY DIAGNOSIS; HUMAN; INFANT; URINALYSIS; URINE COLOR;

ALKAPTONURIA; DIAGNOSIS, DIFFERENTIAL; HOMOGENTISIC ACID; HUMANS; INFANT; MALE; PROGNOSIS; URINALYSIS;

EID: 0033842960     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(00)80194-3     Document Type: Article

References (13)

1. Ueber das Alkapton; Ein neur eitrag zur frage: Welche stoffe des harms konnen kupferedution beuirken?
2. The incidence of alkaptonuria: A study in chemical individuality
3. Le syndrome de Munchhausen par procuration
4. Munchhausen syndrome by proxy: Report of one case with epilepsy
5. Ein fall von allgemeiner Ochronse der Knorpel und knorpelahnichen theile
6. Ueber Ochonose
7. Alkaptonuria
8. Mutation and polymorphism analysis of the human homogentisate 1,2-dioxygenase gene in alkaptonuria patients
9. A novel point mutation associated with alkaptonuria [letter]
10. Capillary electrophoresis for diagnosis of metabolic disease
11. The success of dietary protein restriction in alkaptonuria patients is age-dependent
12. Are we ready to try to cure alkaptonuria?
13. Symptomatic response to ascorbic acid