Assessing the Burden on Caregivers of MECP2 Duplication Syndrome-Reference-Cited by-同舟云学术

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Assessing the Burden on Caregivers of MECP2 Duplication Syndrome

Published:2022-08 Issue: Volume:133 Page:1-8
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Ak Muharrem,Akturk Zekeriya,Bowyer Kristina,Mignon Laurence,Pasupuleti Sasidhar,Glaze Daniel G.,Suter Bernhard,Pehlivan Davut

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference45 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

2. Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls;Hagberg;Acta Paediatr Scand,1985

3. Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies;Sandweiss;Lancet Neurol,2020

4. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome;Meins;J Med Genet,2005

5. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males;Van Esch;Am J Hum Genet,2005

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Parent and caregiver report questionnaires for children and adolescents with intellectual disabilities: a systematic review;International Journal of Developmental Disabilities;2024-08-08

2. MECP2-related disorders while gene-based therapies are on the horizon;Frontiers in Genetics;2024-02-12

3. How Families Manage the Complex Medical Needs of Their Children with MECP2 Duplication Syndrome;Children;2023-07-11

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