Literature DB >> 4018961

The Larsen syndrome occurring in four generations of one family.

D Stanley, N Seymour.   

Abstract

Details of eight (possibly nine) patients with autosomal dominant inheritance of the Larsen Syndrome are reported. They are from four generations of one family and particular reference is made to their complex foot deformities.

Entities:  

Mesh：

Year:  1985        PMID： 4018961     DOI： 10.1007/bf00266871

Source DB:  PubMed          Journal:  Int Orthop        ISSN： 0341-2695            Impact factor:   3.075


  6 in total

1.  Larsen's syndrome: a heritable disorder.

Authors:  E T Habermann; A Sterling; R I Dennis
Journal:  J Bone Joint Surg Am       Date:  1976-06       Impact factor: 5.284

2.  Multiple congenital dislocations associated with characteristic facial abnormality.

Authors:  L J LARSEN; E R SCHOTTSTAEDT; F C BOST
Journal:  J Pediatr       Date:  1950-10       Impact factor: 4.406

3.  Autosomal dominant inheritance in Larsen's syndrome.

Authors:  R Harris; C H Cullen
Journal:  Clin Genet       Date:  1971       Impact factor: 4.438

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

Authors:  R J Latta; C B Graham; J Aase; S M Scham; D W Smith
Journal:  J Pediatr       Date:  1971-02       Impact factor: 4.406

5.  The Larsen syndrome with multiple congenital dislocations and a normal facies.

Authors:  A W Samuel; D R Davies
Journal:  Int Orthop       Date:  1981       Impact factor: 3.075

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

Authors:  H H Steel; E J Kohl
Journal:  J Bone Joint Surg Am       Date:  1972-01       Impact factor: 5.284
  6 in total
  4 in total

1.  A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Authors:  Louise S Bicknell; Claire Farrington-Rock; Yousef Shafeghati; Patrick Rump; Yasemin Alanay; Yves Alembik; Navid Al-Madani; Helen Firth; Mohammad Hassan Karimi-Nejad; Chong Ae Kim; Kathryn Leask; Melissa Maisenbacher; Ellen Moran; John G Pappas; Paolo Prontera; Thomy de Ravel; Jean-Pierre Fryns; Elizabeth Sweeney; Alan Fryer; Sheila Unger; L C Wilson; Ralph S Lachman; David L Rimoin; Daniel H Cohn; Deborah Krakow; Stephen P Robertson
Journal:  J Med Genet       Date:  2006-06-26       Impact factor: 6.318

2.  Mutations responsible for Larsen syndrome cluster in the FLNB protein.

Authors:  D Zhang; J A Herring; S S Swaney; T B McClendon; X Gao; R H Browne; K E Rathjen; C E Johnston; S Harris; N M Cain; C A Wise
Journal:  J Med Genet       Date:  2006-05       Impact factor: 6.318

3.  Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Authors:  Arnold H Menezes; Timothy W Vogel
Journal:  Childs Nerv Syst       Date:  2008-03-28       Impact factor: 1.475

4.  Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.

Authors:  Matthew B Dobbs; Stephanie Boehm; Dorothy K Grange; Christina A Gurnett
Journal:  Clin Orthop Relat Res       Date:  2008-03-06       Impact factor: 4.176
  4 in total

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