Hyperinsulinism and hyperammonaemia

Journal of Inherited Metabolic Disease

Volumn 21, Issue 6, 1998, Pages 671-673

  Al Shamsan, L ^a   Al Essa, M ^b   Al Mutair, A ^b   Al Ashwal, A ^b   Sakati, N ^b   Ozand, P T ^b,c  

^a KING FAHAD NATIONAL GUARD HOSPITAL   (Saudi Arabia)

^b Department of Pediatrics

^c KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYTOIN; VALPROIC ACID;

ADOLESCENT; ARTICLE; CASE REPORT; HUMAN; HYPERAMMONEMIA; HYPERINSULINISM; HYPOGLYCEMIA; INBORN ERROR OF METABOLISM; INSULIN BLOOD LEVEL; INSULINOMA; MALE; MENTAL DEFICIENCY; SEIZURE SUSCEPTIBILITY;

ADOLESCENT; AMMONIA; HUMANS; HYPERINSULINISM; MALE;

EID: 0031752222     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005436701780     Document Type: Article

References (5)

1. Mathew PM, Young JM, Abu-Osba YK, et al (1988) Persistent neonatal hyperinsulinism. Clin Pediatr 27: 148-151.
2. Stanley CA (1997) Hyperinsulinism in infants and children. Pediatr Clin N Am 44: 363-374.
3. Thomas PM, Cote GJ, Hallman DM, Mathew PM (1995) Homozygosity mapping to chromosome lip of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet 56: 416-421.
4. Weinzimer SA, Stanley CA, Berry GT, Yudkoff M, Tuchman M, Thornton PS (1997) A syndrome of congenital hyperinsulinism and hyperammonemia. J Pediatr 130: 661-664.
5. Zammarchi E, Filippi L, Novembre E, Donati MA (1996) Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia. Metabolism 45: 957-960.