Literature DB >> 17890419

Infantile spasms as an epileptic feature of DEND syndrome associated with an activating mutation in the potassium adenosine triphosphate (ATP) channel, Kir6.2.

Nadia Bahi-Buisson1, Monica Eisermann, Sylvie Nivot, Christine Bellanné-Chantelot, Olivier Dulac, Nathalie Bach, Perrine Plouin, Catherine Chiron, Pascale de Lonlay.   

Abstract

Activating mutations in the Kir6.2 subunit of the adenosine triphosphate-sensitive potassium (KATP) channel is a cause of neonatal diabetes associated with various neurological disorders that include developmental delay, epilepsy, and neonatal diabetes (known together as DEND syndrome). This article reports a girl who developed infantile spasms and early onset diabetes mellitus at the age of 3 months and revealed DEND syndrome with a heterozygous activating mutation in Kir6.2. Infantile spasms with hypsarrhythmia on the electroencephalogram were severe and refractory to steroids. Steroids combined with oral sulfonylurea, a drug that closes the ATP-sensitive potassium channel by an independent mechanism, allowed partial and transitory control of the epilepsy. However, the child still exhibited severe encephalopathy and died of aspiration pneumonia. The role of oral sulfonylurea as an anticonvulsant in DEND syndrome associated with Kir6.2 mutation is discussed.

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Year:  2007        PMID: 17890419     DOI: 10.1177/0883073807306272

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  11 in total

1.  Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission.

Authors:  Kathleen Askland; Cynthia Read; Jason Moore
Journal:  Hum Genet       Date:  2008-12-04       Impact factor: 4.132

Review 2.  Infantile spasms: review of the literature and personal experience.

Authors:  Alberto Fois
Journal:  Ital J Pediatr       Date:  2010-02-08       Impact factor: 2.638

Review 3.  Genetic and biologic classification of infantile spasms.

Authors:  Alex R Paciorkowski; Liu Lin Thio; William B Dobyns
Journal:  Pediatr Neurol       Date:  2011-12       Impact factor: 3.372

4.  DEND mutation in Kir6.2 (KCNJ11) reveals a flexible N-terminal region critical for ATP-sensing of the KATP channel.

Authors:  Joseph C Koster; Harley T Kurata; Decha Enkvetchakul; Colin G Nichols
Journal:  Biophys J       Date:  2008-08-15       Impact factor: 4.033

Review 5.  Latest American and European updates on infantile spasms.

Authors:  Andrew L Lux
Journal:  Curr Neurol Neurosci Rep       Date:  2013-03       Impact factor: 5.081

6.  Dual role of K ATP channel C-terminal motif in membrane targeting and metabolic regulation.

Authors:  Crystal F Kline; Harley T Kurata; Thomas J Hund; Shane R Cunha; Olha M Koval; Patrick J Wright; Matthew Christensen; Mark E Anderson; Colin G Nichols; Peter J Mohler
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-15       Impact factor: 11.205

7.  Opening of astrocytic mitochondrial ATP-sensitive potassium channels upregulates electrical coupling between hippocampal astrocytes in rat brain slices.

Authors:  Jiangping Wang; Zhongxia Li; Mei Feng; Keming Ren; Guoxia Shen; Congying Zhao; Xiaoming Jin; Kewen Jiang
Journal:  PLoS One       Date:  2013-02-13       Impact factor: 3.240

8.  Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinism.

Authors:  Kenju Shimomura; Sarah E Flanagan; Brittany Zadek; Mark Lethby; Lejla Zubcevic; Christophe A J Girard; Oliver Petz; Roope Mannikko; Ritika R Kapoor; Khalid Hussain; Mars Skae; Peter Clayton; Andrew Hattersley; Sian Ellard; Frances M Ashcroft
Journal:  EMBO Mol Med       Date:  2009-06       Impact factor: 12.137

9.  The molecular mechanisms and pharmacotherapy of ATP-sensitive potassium channel gene mutations underlying neonatal diabetes.

Authors:  Veronica Lang; Peter E Light
Journal:  Pharmgenomics Pers Med       Date:  2010-11-24

10.  Novel perspectives of super-high dose sulfonylurea and high-dose oral prednisolone in an infant with DEND syndrome due to V64M heterozygote KCNJ11 mutation.

Authors:  Galia Barash; Haim Bassan; Ayelet Livne; Lilach Benyamini; Eli Heyman; Pamela Bowman; Marianna Rachmiel
Journal:  Acta Diabetol       Date:  2021-07-16       Impact factor: 4.280

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