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Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism
OBJECTIVE: Mutations in the KATP channel genes is the most common cause of congenital hyperinsulinism (CHI) of infancy. Our aim was to report the clinical and genetic characteristics, treatment modalities, and long-term prognosis of patients with CHI. METHODS: Clinical and biochemical findings, oper...
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| Publicado no: | J Clin Res Pediatr Endocrinol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Galenos Publishing
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5096476/ https://ncbi.nlm.nih.gov/pubmed/26758964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.2408 |
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