Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Altered Bone Status in Rett Syndrome

3 Jun 2021

Abstract excerpt

Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-linked MECP2 gene, encoding for methyl-CpG binding protein 2 (MeCP2), a multifaceted modulator of gene expression and chromatin organization. Based on the type of mutation, RTT patients exhibit a broad spectrum of clinical phenotypes with various degrees of severity. In addition, as a complex multisystem disease, RTT...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child Nutrition and Feeding Issues
Share to Autism Spectrum Disorder Research
Share to Genetics and Neurodevelopmental Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34205017
DOI: 10.3390/life11060521

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Altered Bone Status in Rett SyndromePMID 34205017Read ↗

Increased Osteoclast Activity Contributes to Bone Resorption and Osteopenia in a Rett Syndrome Mouse ModelSemantic proximity Read ↗

Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome.Semantic proximity Read ↗

Biomechanical properties of bone in a mouse model of Rett syndrome.Semantic proximity Read ↗

Bone mass in Rett syndrome: association with clinical parameters and MECP2 mutations.Semantic proximity Read ↗

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome.Semantic proximity Read ↗

Low bone turnover phenotype in Rett syndrome: results of biochemical bone marker analysis.Semantic proximity Read ↗

Atypical Manifestations of Rett Syndrome: Macrocephaly and Hyperostosis Frontalis Interna in a Female PatientSemantic proximity Read ↗

Atypical Manifestations of Rett Syndrome: Macrocephaly and Hyperostosis Frontalis Interna in a Female PatientSemantic proximity Read ↗

A case report: bone marrow mesenchymal stem cells from a Rett syndrome patient are prone to senescence and show a lower degree of apoptosis.Semantic proximity Read ↗

Patients with Rett syndrome sustain low-energy fractures.Semantic proximity Read ↗

The new bone biology: pathologic, molecular, and clinical correlates.Semantic proximity Read ↗

Rett syndrome: a neurological disorder with metabolic components.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.