Congenital Hyperinsulinism in a Neonate Due to a Novel Homozygous Mutation (ABCC8): A case report

Author(s):
H ParappilH Parappil1, S RahmanS Rahman1,*, A SolimanA Soliman2, A IsmailA Ismail3, I AL BozomI AL Bozom4, K HussainK Hussain5
1Departments of Neonatology, Hamad Medical Corporation, Doha, State of Qatar
2Departments of Endocrinology, Hamad Medical Corporation, Doha, State of Qatar
3Departments of Surgery, Hamad Medical Corporation, Doha, State of Qatar
4Departments of Pathology, Hamad Medical Corporation, Doha, State of Qatar
5Department of Endocrinology, Great Ormand Street, Hospital for Children NHS Trust, London, and The Institute of Child Health, University College, London, UK

International Journal of Endocrinology and Metabolism:Vol. 7, issue 2; e94620
Published online:Jun 30, 2009
Article type:Case Report
Received:May 29, 2019
Accepted:Jun 30, 2009
How to Cite:Parappil H, Rahman S, Soliman A, Ismail A, Bozom IA, et al. Congenital Hyperinsulinism in a Neonate Due to a Novel Homozygous Mutation (ABCC8): A case report. Int J Endocrinol Metab. 2009;7(2):e94620. doi:

Abstract

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