Larsen's syndrome: a skeletal dysplasia with multiple joint dislocations and unusual facies.

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作者信息

Latta R J, Graham C B, Aase J, Scham S M, Smith D W

出版信息

J Pediatr. 1971 Feb;78(2):291-8. doi: 10.1016/s0022-3476(71)80014-8.

DOI:10.1016/s0022-3476(71)80014-8

PMID:5539773

Abstract

摘要

相似文献

Larsen's syndrome: a skeletal dysplasia with multiple joint dislocations and unusual facies.

J Pediatr. 1971 Feb;78(2):291-8. doi: 10.1016/s0022-3476(71)80014-8.

[Larsen's syndrome: congenital dislocation of the knees and other joints, distinctive facies, and, frequently, cleft palate].

Ann Radiol (Paris). 1972 Mar-Apr;15(3):297-328.

[Larsen's syndrome (apropos of 2 cases)].[拉森综合征（附2例报告）]

Pediatrie. 1978 Dec;33(8):775-85.

Multiple congenital dislocations associated with other skeletal anomalies (Larsen's syndrome) in three siblings.三例同胞兄弟姐妹患有与其他骨骼异常相关的多发性先天性脱位（拉森综合征）。

J Bone Joint Surg Am. 1972 Jan;54(1):75-82.

[Larsen's syndrome].[拉森综合征]

Med Welt. 1980 Oct 24;31(43):1548-9.

Pediatric radiologic notes. Case no. 376. Larsen's syndrome (multiple congenital dislocations with characteristic facies).

Mt Sinai J Med. 1974 May-Jun;41(3):492-8.

Roentgen rounds #90. Newborn with club feet and dislocatable hips, knees, and elbows. Campomelic dysplasia.伦琴病例90。患有马蹄内翻足以及髋关节、膝关节和肘关节可脱位的新生儿。弯肢侏儒症。

Orthop Rev. 1987 Sep;16(9):687-90.

[Letter: Larsen's syndrome: congenital multiple dislocations with facial anomalies].

Minerva Pediatr. 1975 Jun 9;27(20):1171-2.

[Larsen's syndrome. Clinical findings and inheritance (author's transl)].[拉森综合征。临床发现与遗传（作者译）]

Arch Fr Pediatr. 1982 Jan;39(1):35-8.

[Diagnosis and treatment of diastrophic dysplasia and Larsen's syndrome in the 1st years of life].[生命第一年中软骨发育不全和拉森综合征的诊断与治疗]

Ortop Travmatol Protez. 1990 Sep(9):56-60.

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Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome.扩展B4GALT7缺乏症的临床谱：具有奠基者效应的纯合p.R270C突变导致留尼汪岛拉森综合征。

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A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delay.一种具有特征性面部特征、骨骼发育不良和发育迟缓的新认识综合征。

Am J Med Genet A. 2012 Aug;158A(8):1815-22. doi: 10.1002/ajmg.a.35445. Epub 2012 Jun 18.

The management of knee dislocation in a child with Larsen syndrome.Larsen综合征患儿膝关节脱位的治疗

Clinics (Sao Paulo). 2011;66(7):1295-9. doi: 10.1590/s1807-59322011000700030.

Images - Extra (too many) carpal bones in Larsen's syndrome.影像——拉森综合征中腕骨过多（额外的）。

Indian J Radiol Imaging. 2009 Apr-Jun;19(2):158-9. doi: 10.4103/0971-3026.50837.

Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.隐性拉森综合征和肱骨-脊柱发育不全中由碳水化合物硫酸转移酶3缺乏引起的先天性关节脱位。

Am J Hum Genet. 2008 Jun;82(6):1368-74. doi: 10.1016/j.ajhg.2008.05.006.

Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.病例报告：一名患有拉森综合征及新型细丝蛋白B突变的患者出现先天性膝关节脱位。

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