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）。 - Suppr

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超能文献

Multiple congenital dislocations associated with other skeletal anomalies (Larsen's syndrome) in three siblings.

作者信息

Steel H H, Kohl E J

出版信息

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

PMID:4626580

Abstract

摘要

相似文献

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: a heritable disorder.拉森综合征：一种遗传性疾病。

J Bone Joint Surg Am. 1976 Jun;58(4):558-61.

Autosomal dominant inheritance in Larsen's syndrome.拉森综合征的常染色体显性遗传。

Clin Genet. 1971;2(2):87-90. doi: 10.1111/j.1399-0004.1971.tb00260.x.

[Larsen's syndrome].[拉森综合征]

Orv Hetil. 1973 Nov 11;114(45):2723-6.

A paradigm for the age-related treatment of knee dislocations in Larsen's syndrome.拉森综合征膝关节脱位的年龄相关性治疗范例。

J Pediatr Orthop. 2000 May-Jun;20(3):396-401.

Clinical features and treatment of joint dislocations in Larsen's syndrome. Report of three cases in one family.

Clin Orthop Relat Res. 1976 Sep(119):206-10.

[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. Report of three cases in the one family, mother and two offspring.拉森综合征。一个家庭中三例病例报告，母亲和两个子女。

Acta Orthop Scand. 1978 Dec;49(6):582-8. doi: 10.3109/17453677808993241.

Larsen's syndrome;拉森综合征

Clin Pediatr (Phila). 1975 Jan;14(1):53-60. doi: 10.1177/000992287501400106.

Larsen's syndrome: four patients belonging to three generations of a Saudi Arabian family.拉森综合征：沙特阿拉伯一个家族三代中的四名患者。

Rev Rhum Engl Ed. 1997 Oct;64(10):538-41.

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Human genetic disorders and knockout mice deficient in glycosaminoglycan.人类遗传疾病和缺乏糖胺聚糖的基因敲除小鼠。

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Human genetic disorders caused by mutations in genes encoding biosynthetic enzymes for sulfated glycosaminoglycans.人类遗传性疾病是由于编码合成硫酸化糖胺聚糖的生物合成酶的基因突变引起的。

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Ehlers-Danlos arthrochalasia type (VIIA-B)--expanding the phenotype: from prenatal life through adulthood.埃勒斯-当洛斯关节过度伸展型（VIIA-B）--扩展表型：从胎儿期到成年期。

Clin Genet. 2012 Aug;82(2):121-30. doi: 10.1111/j.1399-0004.2011.01758.x. Epub 2011 Aug 24.

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.

Significant traumatic atrophy of the spinal cord in connection with severe cervical vertebral body hypoplasia in a boy with Larsen syndrome: a case report and review of the literature.一名患有拉森综合征男孩出现与严重颈椎椎体发育不全相关的脊髓显著创伤性萎缩：病例报告及文献综述

Cases J. 2009 Jun 17;2:6729. doi: 10.4076/1757-1626-2-6729.

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。

Clin Orthop Relat Res. 2008 Jun;466(6):1503-9. doi: 10.1007/s11999-008-0196-5. Epub 2008 Mar 6.

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.一项关于由FLNB基因突变引起的拉森综合征的分子与临床研究。

J Med Genet. 2007 Feb;44(2):89-98. doi: 10.1136/jmg.2006.043687. Epub 2006 Jun 26.

Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome.拇指末节指骨附属骨化中心：拉森综合征的一项额外影像学表现。

Pediatr Radiol. 2006 Sep;36(9):970-3. doi: 10.1007/s00247-006-0217-z. Epub 2006 May 20.

Mutations responsible for Larsen syndrome cluster in the FLNB protein.与拉森综合征相关的突变聚集在FLNB蛋白中。

J Med Genet. 2006 May;43(5):e24. doi: 10.1136/jmg.2005.038695.

Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

Am J Hum Genet. 1995 Nov;57(5):1104-13.

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