Severe developmental delay, epilepsy and neonatal diabetes (DEND) syndrome: a case report

Developmental delay, Epilepsy and Neonatal Diabetes (DEND) syndrome is the most severe form of Permanent Neonatal Diabetes with KCNJ11 gene mutation which accounts for most of the cases. We report the first DEND syndrome in Malaysia with heterozygous missense mutation Q52R at KCNJ11 (Kir6.2) gene wi...

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Bibliographic Details
Main Authors: Muhd Helmi, Muhd Alwi, Hussain, Suhaimi
Format: Article
Language:English
English
Published: ASEAN Federation of Endocrine Societies 2020
Subjects:
Online Access:http://irep.iium.edu.my/80977/2/699-Article%20Text-10041-1-10-20200530.pdf
http://irep.iium.edu.my/80977/3/Scopus%20-%20Document%20details.pdf
http://irep.iium.edu.my/80977/
https://asean-endocrinejournal.org/index.php/JAFES/article/view/699
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