Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype.

Flanagan, S E; Mackay, D J G; Greeley, S A W; McDonald, T J; Mericq, V; Hassing, J; Richmond, E J; Martin, W R; Acerini, C; Kaulfers, A M; Flynn, D P; Popovic, J; Sperling, M A; Hussain, K; Ellard, S; Hattersley, A T

Flanagan, S E; Mackay, D J G; Greeley, S A W; McDonald, T J; Mericq, V; Hassing, J; Richmond, E J; Martin, W R; Acerini, C; Kaulfers, A M; Flynn, D P; Popovic, J; Sperling, M A; Hussain, K; Ellard, S; Hattersley, A T.

Diabetologia ; 56(1): 218-21, 2013 Jan.

Article in En | MEDLINE | ID: mdl-23111732

Subject(s)

Chromosomes, Human, Pair 6/genetics; DNA Methylation; Diabetes Mellitus/congenital; Hypoglycemia/etiology; Infant, Newborn, Diseases/genetics; Infant, Newborn, Diseases/physiopathology; Uniparental Disomy; Chromosome Deletion; Chromosome Duplication; Diabetes Mellitus/genetics; Diabetes Mellitus/metabolism; Diabetes Mellitus/physiopathology; Fathers; Female; Humans; Hypoglycemia/therapy; Infant, Newborn; Infant, Newborn, Diseases/metabolism; Male; Remission, Spontaneous

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Full text: 1 Database: MEDLINE Main subject: Chromosomes, Human, Pair 6 / DNA Methylation / Uniparental Disomy / Diabetes Mellitus / Hypoglycemia / Infant, Newborn, Diseases Limits: Female / Humans / Male / Newborn Language: En Year: 2013 Type: Article

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