DEND - [Developmental delay - epilepsy - neonatal diabetes] syndrome (Q96959): Difference between revisions
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A síndrome DEDN (atraso no desenvolvimento, epilepsia e diabetes neonatal) descreve uma forma grave de diabetes neonatal devido a mutações ativadoras no gene que codifica os canais de potássio sensíveis ao ATP no pâncreas, músculos, nervos e cérebro | |||
| description / en | description / en | ||
DEND (Developmental delay, Epilepsy, and Neonatal Diabetes) syndrome describes a severe form of neonatal diabetes due to activating mutations in the gene encoding ATP-sensitive potassium channels in the pancreas, muscles, nerves and brain | |||
Revision as of 12:59, 16 August 2026
DEND (Developmental delay, Epilepsy, and Neonatal Diabetes) syndrome describes a severe form of neonatal diabetes due to activating mutations in the gene encoding ATP-sensitive potassium channels in the pancreas, muscles, nerves and brain
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_31390672 |
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| English | DEND - [Developmental delay - epilepsy - neonatal diabetes] syndrome |
DEND (Developmental delay, Epilepsy, and Neonatal Diabetes) syndrome describes a severe form of neonatal diabetes due to activating mutations in the gene encoding ATP-sensitive potassium channels in the pancreas, muscles, nerves and brain |
