Discover Community Create You

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

Radiological and clinical analysis of Madelung's deformity in children.

Orthopaedics & traumatology, surgery & research : OTSR - 1 Oct 2014

Huguet S, Leheup B, Aslan M, Muller F, Dautel G, Journeau P

Abstract excerpt

INTRODUCTION: Madelung's deformity is a bone dysplasia that occurs predominantly in adolescent females, characterized by early epiphyseal growth arrest in the medial part of the distal radius. This leads to an upward and medial displacement of the radial joint surface, restricting range of motion...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Follow-Up Studies
Share to Growth Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Osteochondrodysplasias

Share to Radiography

Share to Radius

Share to Short Stature Homeobox Protein

Source

Identifiers

PMID: 25217032
DOI: 10.1016/j.otsr.2014.06.007

Genes

SHOX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25217032-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Radiological and clinical analysis of Madelung's deformity in children.PMID 25217032Read ↗

Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plate.Semantic proximity Read ↗

Clinical and radiological characteristics of 22 children with SHOX anomalies and familial short stature suggestive of Léri-Weill Dyschondrosteosis.Semantic proximity Read ↗

X-linked frontometaphyseal dysplasia with severe scoliosis and spinal cord compromise in an Indian boy.Semantic proximity Read ↗

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.Semantic proximity Read ↗

Increased cortical area and thickness in the distal radius in subjects with SHOX-gene mutation.Semantic proximity Read ↗

Windswept lower limb deformities in patients with hypophosphataemic rickets.Semantic proximity Read ↗

Phenotypes Associated with SHOX Deficiency.Semantic proximity Read ↗

Phenotypes Associated with SHOX DeficiencySemantic proximity Read ↗

Auxological and anthropometric evaluation in skeletal dysplasias.Semantic proximity Read ↗

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.Semantic proximity Read ↗

Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article.Semantic proximity Read ↗

Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome.Semantic proximity Read ↗

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