Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family

Author:

Babiker Omer,Flanagan Sarah E.,Ellard Sian,Girim Hesham Al,Hussain Khalid,Senniappan Senthil

Abstract

AbstractHyperinsulinaemic hypoglycaemia (HH) is caused by mutations in the key genes involved in regulation of insulin secretion from the pancreatic β-cells and mutations in

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Reference48 articles.

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4. Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant katp channel mutations;Pinney;J Clin Invest,2008

5. hydroxyacyl - coenzyme a dehydrogenase deficiency and hyperinsulinemic hypoglycemia : characterization of a novel mutation and severe dietary protein sensitivity;Kapoor;J Clin Endocrinol Metab,2009

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