Literature DB >> 8923936

Distal arthrogryposis type 1: clinical analysis of a large kindred.

M Bamshad1, J F Bohnsack, L B Jorde, J C Carey.   

Abstract

We describe the clinical findings of 15 individuals in a large kindred affected with distal arthrogryposis type 1A (DA1A). The most consistent findings among individuals were overlapping fingers at birth, abnormal digital flexion creases, and foot deformities, including talipes equinovarus and vertical talus. There was marked intrafamilial variation in the expression of DA1A. Linkage mapping of the locus for DA1A suggests that the use of strict diagnostic criteria excludes unaffected individuals rigorously, but can produce incomplete ascertainment of affected individuals. In the context of an affected family, the range of phenotypes consistent with a diagnosis of DA1A needs to be expanded.

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Year:  1996        PMID: 8923936     DOI: 10.1002/(SICI)1096-8628(19961111)65:4<282::AID-AJMG7>3.0.CO;2-R

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

1.  Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1.

Authors:  Christina A Gurnett; David M Desruisseau; Kevin McCall; Ryan Choi; Zachary I Meyer; Michael Talerico; Sara E Miller; Jeong-Sun Ju; Alan Pestronk; Anne M Connolly; Todd E Druley; Conrad C Weihl; Mathew B Dobbs
Journal:  Hum Mol Genet       Date:  2010-01-02       Impact factor: 6.150

2.  A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter.

Authors:  P A Krakowiak; J R O'Quinn; J F Bohnsack; W S Watkins; J C Carey; L B Jorde; M Bamshad
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

3.  Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis.

Authors:  Jessica X Chong; Jared C Talbot; Emily M Teets; Samantha Previs; Brit L Martin; Kathryn M Shively; Colby T Marvin; Arthur S Aylsworth; Reem Saadeh-Haddad; Ulrich A Schatz; Francesca Inzana; Tawfeg Ben-Omran; Fatima Almusafri; Mariam Al-Mulla; Kati J Buckingham; Tamar Harel; Hagar Mor-Shaked; Periyasamy Radhakrishnan; Katta M Girisha; Shalini S Nayak; Anju Shukla; Klaus Dieterich; Julien Faure; John Rendu; Yline Capri; Xenia Latypova; Deborah A Nickerson; David M Warshaw; Paul M L Janssen; Sharon L Amacher; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2020-07-23       Impact factor: 11.025

4.  Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.

Authors:  Sandy S Sung; Anna-Marie E Brassington; Kathryn Grannatt; Ann Rutherford; Frank G Whitby; Patrycja A Krakowiak; Lynn B Jorde; John C Carey; Mike Bamshad
Journal:  Am J Hum Genet       Date:  2003-03       Impact factor: 11.025

5.  Skeletal muscle contractile gene (TNNT3, MYH3, TPM2) mutations not found in vertical talus or clubfoot.

Authors:  Christina A Gurnett; Farhang Alaee; David Desruisseau; Stephanie Boehm; Matthew B Dobbs
Journal:  Clin Orthop Relat Res       Date:  2009-01-14       Impact factor: 4.176

6.  Spectrum of mutations that cause distal arthrogryposis types 1 and 2B.

Authors:  Anita E Beck; Margaret J McMillin; Heidi I S Gildersleeve; Phillip R Kezele; Kathryn M Shively; John C Carey; Michael Regnier; Michael J Bamshad
Journal:  Am J Med Genet A       Date:  2013-02-07       Impact factor: 2.802

7.  Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis.

Authors:  Bertrand Coste; Gunnar Houge; Michael F Murray; Nathan Stitziel; Michael Bandell; Monica A Giovanni; Anthony Philippakis; Alexander Hoischen; Gunnar Riemer; Unni Steen; Vidar Martin Steen; Jayanti Mathur; James Cox; Matthew Lebo; Heidi Rehm; Scott T Weiss; John N Wood; Richard L Maas; Shamil R Sunyaev; Ardem Patapoutian
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-04       Impact factor: 11.205

  7 in total

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