Table 1.
Transient nature | |
Infant born to diabetic mother (gestational or permanent diabetes) | |
Intrauterine growth retardation | |
Rhesus disease | |
Perinatal asphyxia | |
Erythroblastosis fetalis | |
Childhood onset – persistent nature | |
Congenital causes | Genetic mutations in: |
ABCC8, KCNJ11, GDH, HADH, GCK, SLC16A1, GLUD1, UCP2, HNF4A, HNF1A, HK1, PGM1, PPM2 | |
Syndromic causes | Beckwith–Wiedemann |
Mosaic Turner | |
Timothy | |
Soto | |
Simpson–Golabi–Behmel | |
Kabuki | |
Patau – Trisomy 13 | |
Rubenstein Taybi | |
Costello | |
Congenital disorders of glycosylation (CDG types 1A, 1B and 1D) | |
Congenital hypoventilation | |
Poland | |
Childhood/adult onset – persistent nature | |
Tumours | IGF-2-oma |
Benign and malignant insulinoma | |
Non-islet cell tumour hypoglycaemia | |
Drug-use related | Glinides |
Insulin | |
Sulphonylureas | |
Factitious hypoglycaemia | Munchausen syndrome by proxy |
Postprandial | Dumping syndrome |
Post gastric by-pass surgery for morbid obesity Non-insulinoma pancreatogenous hypoglycaemia |
|
Other causes | Auto-antibodies against insulin |
Insulin resistance syndrome |