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Bilateral Severe Genu Varum in Dyggve-Melchior-Clausen Syndrome - A Case Report
INTRODUCTION: Dyggve-Melchior-Clausen (DMC) syndrome was described in 1962 as an autosomal recessive type of spondyloepimetaphyseal dysplasia associated with mental retardation. Dymeclin (DYM) gene on chromosome 18q12.1 that encodes for DYM protein which is expressed in cartilage, bone, and brain is...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Orthopaedic Research Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686494/ https://www.ncbi.nlm.nih.gov/pubmed/35004383 http://dx.doi.org/10.13107/jocr.2021.v11.i08.2378 |