Permanent neonatal diabetes

Israel Medical Association Journal

Volumn 6, Issue 5, 2004, Pages 290-291

  Bakri, Doua ^a   Gershoni Baruch, Ruth ^a   Shehadeh, Naim ^a  

^a Meyer's Children's Hospital   (Israel)

Author keywords

Diabetes; Glucokinase; Insulin promoter factor 1; Mutation; Neonatal

Indexed keywords

C PEPTIDE; GLUCOSE; INSULIN; REPAGLINIDE;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 6; DIABETES MELLITUS; DISEASE ASSOCIATION; GENE EXPRESSION; GENE MUTATION; GLUCOSE BLOOD LEVEL; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRAUTERINE GROWTH RETARDATION; NEWBORN DISEASE; ORAL GLUCOSE TOLERANCE TEST; SCHOOL CHILD;

ADULT; CHILD; DIABETES MELLITUS, TYPE 1; GENOTYPE; GLUCOKINASE; HUMANS; HYPOGLYCEMIC AGENTS; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; INSULIN;

EID: 2442527897     PISSN: 15651088     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Shield JP. Neonatal diabetes: new insights into etiology and implications. Horm Res 2000;53(Suppl. S1):7-11.
2. Stoffers DA, Zinkin Nt, Stanojevic V, Clarke WL, Habener JF. Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF-1 gene coding sequence. Nat Genet 1997;15:106-10.
3. Njolstad P., Sovik O, Cuesta-Munoz A, Bjokhaug L, Massa O, Barbetti F. Neonatal diabetes mellitus due to complete glucokinase deficiency. N Engl J Med 2001;344:1588-92.
4. Njolstad PR, Sagen JV, Bjokhaugh L, et al. Permanent neonatal diabetes caused by glucokinase deficiency. Diabetes 2003;52:2854-60.
5. Shehadeh N, Gershoni-Baruck R, Mandel H, Nutenko I, Etzioni A. Congenital permanent diabetes: a different type of diabetes? Acta Paediatr 1996;85:1415-17.