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FOXG1 syndrome

Rett syndrome, congenital variant
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "FOXG1 syndrome" returned 3 free, full-text review articles. First few results:
-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms.
Last Updated: Feb 25, 2020

Individuals with mutations in forkhead box G1 () belong to a distinct clinical entity, termed "-related encephalopathy". There are two clinical phenotypes/syndromes identified in -related encephalopathy, duplications and deletions/intragenic mutations. In children with deletions or ...

Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathies.
Last Updated: Dec 04, 2012

Rett syndrome is an X-linked neurodevelopmental disorder that manifests in early childhood with developmental stagnation, and loss of spoken language and hand use, with the development of distinctive hand stereotypies, severe cognitive impairment, and autistic features. About 60% ...

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3 Free Review Articles 5 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "FOXG1 syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "FOXG1 syndrome" returned 10 free, full-text research articles. First few results:
In Silico Study of Rett Syndrome Treatment-Related Genes, , , and , by Evolutionary Classification and Disordered Region Assessment.
Last Updated: Apr 13, 2020

Rett syndrome (RTT), a neurodevelopmental disorder, is mainly caused by mutations in methyl CpG-binding protein 2 (), which has multiple functions such as binding to methylated DNA or interacting with a transcriptional co-repressor complex. It has been established that alterations ...

Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Last Updated: Feb 25, 2020

FOXG1 syndrome is a rare neurodevelopmental disorder associated with heterozygous variants or chromosomal microaberrations in 14q12. The study aimed at assessing the scope of structural cerebral anomalies revealed by neuroimaging to delineate the genotype and neuroimaging phenotype associations.

Precisely controlling endogenous protein dosage in hPSCs and derivatives to model FOXG1 syndrome.
Last Updated: Mar 09, 2020

Dosage of key regulators impinge on developmental disorders such as FOXG1 syndrome. Since neither knock-out nor knock-down strategy assures flexible and precise protein abundance control, to study hypomorphic or haploinsufficiency expression remains challenging. We develop a system ...

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