Neonatal diabetes mellitus with recurrent hepatitis [4]

Indian Journal of Pediatrics

Volumn 73, Issue 5, 2006, Pages 451-452

  Suresh, N ^a   Ganesh, R ^a   Eswararaja, T ^a   Vasanthi, T ^a   Sankar, Janani ^a   Sathiasekaran, Malathi ^a  

^a KANCHI KAMAKOTI CHILDS TRUST HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN;

ANAMNESIS; BLOOD ANALYSIS; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DIABETES MELLITUS; DISEASE ASSOCIATION; FEMALE; GLUCOSE BLOOD LEVEL; HEPATITIS; HEPATOSPLENOMEGALY; HUMAN; INFANT; JAUNDICE; LABORATORY TEST; LETTER; LIVER BIOPSY; LIVER FUNCTION TEST; NEWBORN DISEASE; NEWBORN SCREENING; PHYSICAL EXAMINATION; RECURRENT DISEASE; STEATOSIS; SYMPTOMATOLOGY; THORAX RADIOGRAPHY; INSULIN DEPENDENT DIABETES MELLITUS; NEWBORN; SYNDROME;

DIABETES MELLITUS, TYPE 1; FEMALE; HEPATITIS; HUMANS; INFANT; INFANT, NEWBORN; RECURRENCE; SYNDROME;

EID: 33746662921     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02758578     Document Type: Letter

References (8)

1. Bappal B, Raghupathy P, de silva V, Khushiby SM. Permanent neonatal diabetes mellitus. Clinical presentation and epidemiology in Oman. Arch Dis Child Fetal Neonatal Ed 1999; 80: 209-212.
2. Porter JR, Shaw NJ, Barrett TG. Permanent neonatal diabetes in an asian infant. Journal of Pediatr 2005; 146 : 47-49.
3. Massa O, Iafusco D, D'Amato E. KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes. Hum Mutat 2005; 25 : 22-27.
4. Menon PSN, Khatwa UA. Diabetes mellitus in newborns and infants. Indian J Pediatr 2000; 67 : 443-448.
5. Wolcott CD, Rallison ML. Infancy - onset diabetes mellitus and multiple epiphyseal dysplasia J. Pediatr 1972; 80 : 292-297.
6. Abbas BB, Shabib S. Wolcott Rallison syndrome: Clinical, radiological and histological findings in a Saudi child. Annals of Saudi Medicine 2001; 21: 1-2.
7. Brickwood S, Bonthron DT, Gazali-LIAI et al. Wolcott-Rallison syndrome: pathogenic insights in to neonatal diabetes from new mutation and expression studies of EIF2AK3. J Med Genet 2003; 40: 685-689.
8. Iyer S, Korada M, Rainbow L et al. Wolcott - Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature. Acta Paeditr 2004; 93: 1195-1201.