Rett-like Phenotypes in <i>HNRNPH2</i>-Related Neurodevelopmental Disorder

Rett-like Phenotypes in <i>HNRNPH2</i>-Related Neurodevelopmental Disorder

Rett Syndrome (RTT) is a neurodevelopmental disorder with a prevalence of 1:10,000 to 15,000 females worldwide. Classic Rett Syndrome presents in early childhood with a period of developmental regression, loss of purposeful hand skills along with hand stereotypies, gait abnormalities, and loss of ac...

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Bibliographic Details
Main Authors: Joseph Nicho Gonzalez, Sylvie Goldman, Melissa T. Carter, Jennifer M. Bain
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Genes
Subjects:
<i>HNRNPH2</i>
<i>HNRNPH2</i>-related neurodevelopmental disorder (<i>HNRNPH2</i>-RNDD)
neurodevelopmental disorder (NDD)
Rett Syndrome
neurodevelopmental disorder
Rett-like phenotypes
Online Access:https://www.mdpi.com/2073-4425/14/6/1154

Internet

https://www.mdpi.com/2073-4425/14/6/1154

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