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Orthopaedic manifestations in de Barsy syndrome.

作者信息

Stanton R P, Rao N, Scott C I

机构信息

Alfred I. duPont Institute, Wilmington, Delaware 19899.

出版信息

J Pediatr Orthop. 1994 Jan-Feb;14(1):60-2. doi: 10.1097/01241398-199401000-00013.

DOI:10.1097/01241398-199401000-00013
PMID:8113374
Abstract

de Barsy syndrome is a rare, genetically transmitted condition characterized by severe cutis laxa, joint hypermobility, growth retardation, mental retardation, and characteristic facies. Affected individuals have many orthopaedic manifestations, including developmental dysplasia of the hip, scoliosis, multiple joint dislocations and subluxations, and congenital vertical talus. The management of the orthopaedic manifestations of this syndrome is presented in two typical cases.

摘要

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引用本文的文献

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De Barsy Syndrome: A Case Report of a Rare Genetic Disorder.德巴尔西综合征：一种罕见遗传性疾病的病例报告。
Cureus. 2023 Jan 2;15(1):e33280. doi: 10.7759/cureus.33280. eCollection 2023 Jan.
2
A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited.一名印度儿童的皮肤松弛症5年病程：再探德巴尔西综合征
Indian J Dermatol. 2016 Jan-Feb;61(1):81-4. doi: 10.4103/0019-5154.174031.
3
A new approach to the treatment of congenital vertical talus.先天性垂直距骨的一种新治疗方法。
J Child Orthop. 2007 Sep;1(3):165-74. doi: 10.1007/s11832-007-0037-1. Epub 2007 Aug 1.