Musculocontractural type of Ehlers-Danlos syndrome with novel CHST14 pathogenic variant in two siblings.

IF 1.2 4区 医学 Q3 DERMATOLOGY Pediatric Dermatology Pub Date : 2024-11-01 Epub Date: 2024-06-16 DOI:10.1111/pde.15653
Aswanth Ks, Namrata Sarkar, Riti Bhatia, Vivek Singh, Shruti Sharma, Prashant Kumar Verma
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Abstract

Musculocontractural Ehlers-Danlos syndrome (MC-EDS) is a rare entity worldwide with underlying pathogenic variant in the carbohydrate sulfotransferase 14 (CHST14) gene. Previous reports of the same entity from India were of two unrelated cases. Ours is the first report of two siblings in an Indian family with craniofacial dysmorphism and distal arthrogryposis with a clinical diagnosis of EDS, where an underlying pathogenic variant in CHST14 was detected by exome sequencing.

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两个兄弟姐妹中的埃勒斯-丹洛斯综合征肌肉挛缩型伴有新型 CHST14 致病变异体。
肌肉挛缩性艾勒斯-丹洛斯综合征(MC-EDS)是一种全球罕见的疾病,其潜在的致病基因是碳水化合物磺基转移酶 14(CHST14)。此前,印度曾报道过两例无关联的相同病例。我们首次报告了一个印度家庭中的两个兄弟姐妹,他们患有颅面畸形和远端关节发育不良,临床诊断为 EDS,并通过外显子组测序发现了 CHST14 基因的潜在致病变体。
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来源期刊
Pediatric Dermatology
Pediatric Dermatology 医学-皮肤病学
CiteScore
3.20
自引率
6.70%
发文量
269
审稿时长
1 months
期刊介绍: Pediatric Dermatology answers the need for new ideas and strategies for today''s pediatrician or dermatologist. As a teaching vehicle, the Journal is still unsurpassed and it will continue to present the latest on topics such as hemangiomas, atopic dermatitis, rare and unusual presentations of childhood diseases, neonatal medicine, and therapeutic advances. As important progress is made in any area involving infants and children, Pediatric Dermatology is there to publish the findings.
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