Literature DB >> 24458798

Long-term observation of a patient with dominant omodysplasia.

Barbara L Gordon1, Neena L Champaigne, R Curtis Rogers, Jaime L Frias, Jules G Leroy.   

Abstract

We report on the natural history of a female with dominant omodysplasia, a rare osteochondrodysplasia with short stature, rhizomelia of the extremities (upper extremities more affected), and short first metacarpals. The proband had normal molecular analysis of the glypican 6 gene (GPC6), which was recently reported as a candidate for autosomal recessive omodysplasia. The findings in this patient were compared to other known and suspected cases of autosomal dominant omodysplasia. Mild rhizomelic shortening of the lower extremities has not been previously reported.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  bicornuate uterus; glypican 6; omodysplasia; rhizomelia

Mesh:

Substances:

Year:  2014        PMID: 24458798     DOI: 10.1002/ajmg.a.36408

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  5 in total

1.  A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia.

Authors:  Howard M Saal; Cynthia A Prows; Iris Guerreiro; Milene Donlin; Luke Knudson; Kristen L Sund; Ching-Fang Chang; Samantha A Brugmann; Rolf W Stottmann
Journal:  Hum Mol Genet       Date:  2015-03-10       Impact factor: 6.150

2.  A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia.

Authors:  Seval Türkmen; Malte Spielmann; Nilay Güneş; Alexej Knaus; Ricarda Flöttmann; Stefan Mundlos; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2017-09-08

3.  Dominant omodysplasia-A sporadic case-A new case report and review of the literature.

Authors:  Aidin Arabzadeh; Behnam Baghianimoghadam; Mohammad Hossein Nabian; Yousef Fallah; Mohammad Mehdi Ebrahimnasab
Journal:  Clin Case Rep       Date:  2022-08-03

4.  Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations.

Authors:  Hannah E Warren; Raymond J Louie; Michael J Friez; Jaime L Frías; Jules G Leroy; Jürgen W Spranger; Steven A Skinner; Neena L Champaigne
Journal:  Clin Case Rep       Date:  2018-10-15

5.  Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability.

Authors:  Chaofan Zhang; Angad Jolly; Brian J Shayota; Juliana F Mazzeu; Haowei Du; Moez Dawood; Patricia Celestino Soper; Ariadne Ramalho de Lima; Bárbara Merfort Ferreira; Zeynep Coban-Akdemir; Janson White; Deborah Shears; Fraser Robert Thomson; Sarah Louise Douglas; Andrew Wainwright; Kathryn Bailey; Paul Wordsworth; Mike Oldridge; Tracy Lester; Alistair D Calder; Katja Dumic; Siddharth Banka; Dian Donnai; Shalini N Jhangiani; Lorraine Potocki; Wendy K Chung; Sara Mora; Hope Northrup; Myla Ashfaq; Jill A Rosenfeld; Kati Mason; Lynda C Pollack; Allyn McConkie-Rosell; Wei Kelly; Marie McDonald; Natalie S Hauser; Peter Leahy; Cynthia M Powell; Raquel Boy; Rachel Sayuri Honjo; Fernando Kok; Lucia R Martelli; Vicente Odone Filho; Donna M Muzny; Richard A Gibbs; Jennifer E Posey; Pengfei Liu; James R Lupski; V Reid Sutton; Claudia M B Carvalho
Journal:  HGG Adv       Date:  2021-12-03
  5 in total

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