Transient neonatal diabetes as a presentation of fanconi-bickel syndrome

Acta Medica Iranica

Volumn 50, Issue 12, 2012, Pages 836-838

  Setoodeh, Aria ^a,b   Rabbani, Ali ^a,b  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Fanconi bickel syndrome; Hypophosphatemic rickets; Neonatal diabetes; Severe short stature

Indexed keywords

ISOPHANE INSULIN;

ARTICLE; CASE REPORT; CHILD; DIABETIC KETOACIDOSIS; FANCONI BICKEL SYNDROME; FEMALE; FOLLOW UP; GENE MUTATION; GLYCOGEN STORAGE DISEASE; HEPATOMEGALY; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; HYPOGLYCEMIA; HYPOPHOSPHATEMIC RICKETS; INTRON; LIVER BIOPSY; NEWBORN DIABETES MELLITUS; PATIENT REFERRAL; SCHOOL CHILD; SHORT STATURE; SLC2 A 2 GENE; TRANSIENT NEWBORN DIABETES MELLITUS; URINALYSIS;

CHILD; CONSANGUINITY; DIABETES MELLITUS; DIABETIC KETOACIDOSIS; DNA MUTATIONAL ANALYSIS; FANCONI SYNDROME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GLUCOSE TRANSPORTER TYPE 2; HUMANS; HYPOGLYCEMIC AGENTS; INFANT, NEWBORN; INSULIN; MUTATION; PHENOTYPE;

EID: 84872693401     PISSN: 00446025     EISSN: 17359694     Source Type: Journal    
DOI: None     Document Type: Article

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