| Literature DB >> 30249733 |
Sapna Sandal1, Anupriya Kaur2, Inusha Panigrahi3.
Abstract
Musculocontractural type of Ehlers-Danlos syndrome (MC-EDS) is a recently recognised connective tissue disorder. MC-EDS is caused by homozygous or compound heterozygous mutation in the carbohydrate sulfotransferase 14 (CHST14) gene on chromosome 15q15. Herein, we report a case of a 3-year-old boy with MC-EDS in whom a novel mutation in the CHST14 gene was discovered. Besides being the second report of this rare disorder from India, the child till 3 years has not had any bleeding tendency as described in the earlier reports of this disorder. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: developmental paediatrocs; genetics; musculoskeletal and joint disorders
Mesh:
Substances:
Year: 2018 PMID: 30249733 DOI: 10.1136/bcr-2018-226165
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X