A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

Unlike other congenital fatty acid oxidation defects, short-chain L-3-hydroxyacyl-CoA (SCHAD, HADH) deficiency is characterised by hypoglycemia with hyperinsulinism in the neonatal or infancy periods. The long-term and detailed clinical progression of the disease is largely unknown with almost 40 pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Çamtosun, Emine, Flanagan, Sarah E., Ellard, Sian, Şıklar, Zeynep, Hussain, Khalid, Kocaay, Pınar, Berberoğlu, Merih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563187/
https://www.ncbi.nlm.nih.gov/pubmed/26316438
http://dx.doi.org/10.4274/jcrpe.1963

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563187/
https://www.ncbi.nlm.nih.gov/pubmed/26316438
http://dx.doi.org/10.4274/jcrpe.1963

Ejemplares similares