Literature DB >> 7977470

Desbuquois syndrome: clinical, radiographic, and morphologic characterization.

M Shohat1, R Lachman, H E Gruber, Y E Hsia, M S Golbus, D R Witt, A Bodell, C R Bryke, W A Hogge, D L Rimoin.   

Abstract

To further characterize the clinical, radiographic and chondro-osseous morphologic changes in the Desbuquois syndrome, 7 patients from three sibships are described. They all had prenatal onset severe rhizomelic and mesomelic shortness with marked joint laxity and marked micrognathia. Radiographic changes were distinct, consisting of a supernumerary ossification center between the proximal phalanx of the index finger and the second metacarpal, and variable thumb changes. The femoral necks showed enlargement of the lesser trochanter with metaphyseal breaking, producing a characteristic "monkey wrench" (Swedish key) appearance. Growth plate cartilage showed dilated cisterns of rough endoplasmic reticulum in reserve zone chondrocytes. Three of the 7 cases were diagnosed prenatally by second trimester ultrasound and one case by fetoscopy. This syndrome exhibits significant phenotypic variability and must be differentiated from the Catel-Manzke syndrome which exhibits similar radiographic changes in the hands.

Entities:  

Mesh:

Year:  1994        PMID: 7977470     DOI: 10.1002/ajmg.1320520104

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


  8 in total

1.  Congenital Pseudarthrosis of Index Metacarpal Bone Treated with Distraction Osteogenesis Followed by Autologous Grafting.

Authors:  Aziz Atik; Selahattin Ozyurek; Gokhan Meric; Serdar Sargin; Ozkan Kose; Ali Engin Ulusal
Journal:  J Hand Microsurg       Date:  2014-03-27

2.  Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene.

Authors:  Franco Laccone; Katharina Schoner; Birgit Krabichler; Britta Kluge; Robin Schwerdtfeger; Bernt Schulze; Johannes Zschocke; Helga Rehder
Journal:  Eur J Hum Genet       Date:  2011-06-08       Impact factor: 4.246

3.  A case of skeletal dysplasia with advanced carpal ossification and "monkey wrench" appearance of the femora: mild Desbuquois dysplasia?

Authors:  G Nishimura; S Sato; T Ogata; S Tamai; T Hasegawa; N Matsuo
Journal:  Eur J Pediatr       Date:  1996-12       Impact factor: 3.183

4.  Identification of CANT1 mutations in Desbuquois dysplasia.

Authors:  Céline Huber; Bénédicte Oulès; Marta Bertoli; Mounia Chami; Mélanie Fradin; Yasemin Alanay; Lihadh I Al-Gazali; Margreet G E M Ausems; Pierre Bitoun; Denise P Cavalcanti; Alexander Krebs; Martine Le Merrer; Geert Mortier; Yousef Shafeghati; Andrea Superti-Furga; Stephen P Robertson; Carine Le Goff; Andrea Onetti Muda; Patrizia Paterlini-Bréchot; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2009-10-22       Impact factor: 11.025

5.  First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous CANT1 Mutations.

Authors:  Manal M Thomas; Engy A Ashaat; Ghada A Otaify; Samira Ismail; Mona L Essawi; Mohamed S Abdel-Hamid; Heba A Hassan; Sonia A Alsaiedi; Mona Aglan; Mona O El Ruby; Samia Temtamy
Journal:  Mol Syndromol       Date:  2021-07-22

6.  CANT1 deficiency in a mouse model of Desbuquois dysplasia impairs glycosaminoglycan synthesis and chondrocyte differentiation in growth plate cartilage.

Authors:  Kazuki Kodama; Hiroaki Takahashi; Nobuyasu Oiji; Kenta Nakano; Tadashi Okamura; Kimie Niimi; Eiki Takahashi; Long Guo; Shiro Ikegawa; Tatsuya Furuichi
Journal:  FEBS Open Bio       Date:  2020-04-23       Impact factor: 2.693

7.  Radiographic findings of Desbuquois dysplasia.

Authors:  Meltem Özdemir; Rasime Pelin Kavak
Journal:  BJR Case Rep       Date:  2020-11-02

8.  Synophyrs, curly eyelashes and Ptyrigium colli in a girl with Desbuquois dysplasia: a case report and review of the literature.

Authors:  Ali Al Kaissi; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2009-09-15
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.