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X-linked Spondyloepiphyseal Dysplasia Tarda with Mutation in TRAPPC2Gene: First Report from India

INTRODUCTION: X-linked spondyloepiphyseal dysplasia tarda(SEDT) is a type of shorttrunk skeletal dysplasia, occurring in males due to mutation in TRAPPC2 gene. CASE REPORT: We describe a large Indian family with multiple males affected with X-linked SEDT. The affected individuals presented with disp...

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Detalhes bibliográficos
Publicado no:J Orthop Case Rep
Main Authors: Tamhankar, Parag M, Kulkarni, Abhishek, Vasudevan, Lakshmi
Formato: Artigo
Idioma:Inglês
Publicado em: Indian Orthopaedic Research Group 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7476708/
https://ncbi.nlm.nih.gov/pubmed/32953644
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.13107/jocr.2020.v10.i02.1670
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