Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia.

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Authors
Senniappan, S.
Sadeghizadeh, A.
Flanagan, Sarah
Ellard, Sian
Hashemipour, M.
Hosseinzadeh, M.
Salehi, M.
Hussain, K.
Issue Date
2015
Type
Journal Article
Language
en
Keywords
Wessex Classification Subject Headings::Oncology. Pathology.::Genetics , Wessex Classification Subject Headings::Endocrinology::Diabetes
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Organizational Units
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Alternative Title
Hyperinsulinaemic hypoglycaemia (HH) is a group of clinically and genetically heterogeneous disorders characterized by unregulated insulin secretion. Abnormalities in nine different genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A, UCP2 and HNF1A) have been reported in HH, the most common being ABCC8 and KCNJ11. We describe the genetic aetiology and phenotype of Iranian patients with HH.
Description
Citation
Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia. 2015, 8:350 BMC Res Notes
Publisher
BioMed Central
License
Archived with thanks to BMC research notes
Journal
BMC Research Notes
Volume
Issue
PubMed ID
ISSN
1756-0500
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