埃勒斯-丹洛斯综合征
结缔组织病
医学
先天性疾病
外显子
复合杂合度
突变
遗传学
基因
病理
外科
生物
作者
Sapna Sandal,Anupriya Kaur,Inusha Panigrahi
出处
期刊:Case Reports
[BMJ]
日期:2018-09-23
卷期号:: bcr-226165
被引量:10
标识
DOI:10.1136/bcr-2018-226165
摘要
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.
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