Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child-Reference-Cited by-同舟云学术

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Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child

Published:2023-10-04 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

El Mouhi Hinde,Abbassi Meriame,Sayel Hanane,Trhanint Said,Natiq Abdelhafid,El Hejjioui Brahim,Jalte Merym,Ahmadi Youssef,Chaouki Sana

Publisher

Springer Science and Business Media LLC

Subject

Aerospace Engineering

Reference18 articles.

1. Intellectual disability and language disorder;Marrus N;Child Adolesc Psychiatr Clin N Am,2017

2. The genetic basis of non-syndromic intellectual disability: a review;Kaufman L;J Neurodev Disord,2010

4. A systematic review of neuropsychiatric comorbidities in patients with both epilepsy and intellectual disability;van Ool JS;Epilepsy Behav,2016

5. GRIN2B-related neurodevelopmental disorder. Synonym: GRIN2B encephalopathy;Platzer K,1993

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1. The Genetic Facets of Dravet Syndrome: Recent Insights;Annals of Child Neurology;2024-04-01

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