Literature DB >> 25252066

Case of Desbuquois dysplasia type 1: potentially lethal skeletal dysplasia.

Shinkai Inoue1, Atsushi Ishii, Goro Shirotani, Makoto Tsutsumi, Eiji Ohta, Masatoshi Nakamura, Toshiko Mori, Takahito Inoue, Gen Nishimura, Atsushi Ogawa, Shinichi Hirose.   

Abstract

We report a boy with Desbuquois dysplasia type 1. He had the typical skeletal changes: a "Swedish key" appearance of the proximal femora; advanced carpal ossification and other distinctive features of the hand, including an extra-ossification center at the base of the proximal phalanx of the index and middle fingers; dislocation of the metacarpophalangeal joint of the index finger; and bifid distal phalanx of the thumb. In addition, he presented with very severe prenatal growth failure, respiratory distress as a neonate, subsequent failure to thrive and susceptibility to airway infection, and sudden death in early childhood. Molecular analysis identified homozygous 1 bp deletion in the Calcium-Activated Nucleotidase 1 gene (CANT1). To our knowledge, this is the first report of Desbuquois dysplasia type 1 in Japan. Our experience suggests potential lethality in the disorder.
© 2014 Japan Pediatric Society.

Entities:  

Keywords:  CANT1 gene; Desbuquois dysplasia; diagnosis; fatal outcome; radiographic characterization

Mesh:

Year:  2014        PMID: 25252066     DOI: 10.1111/ped.12383

Source DB:  PubMed          Journal:  Pediatr Int        ISSN: 1328-8067            Impact factor:   1.524


  6 in total

1.  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

2.  Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis.

Authors:  Alicia B Byrne; Shuji Mizumoto; Peer Arts; Patrick Yap; Jinghua Feng; Andreas W Schreiber; Milena Babic; Sarah L King-Smith; Christopher P Barnett; Lynette Moore; Kazuyuki Sugahara; Hatice Mutlu-Albayrak; Gen Nishimura; Jan E Liebelt; Shuhei Yamada; Ravi Savarirayan; Hamish S Scott
Journal:  J Med Genet       Date:  2020-01-27       Impact factor: 6.318

3.  Cloning, expression and enzyme activity delineation of two novel CANT1 mutations: the disappearance of dimerization may indicate the change of protein conformation and even function.

Authors:  Hong-Dan Wang; Liang-Jie Guo; Zhan-Qi Feng; Da-Wei Zhang; Meng-Ting Zhang; Yue Gao; Chuan-Liang Chen; Bo-Feng Zhu
Journal:  Orphanet J Rare Dis       Date:  2020-09-09       Impact factor: 4.123

4.  Prenatal diagnosis of fetal skeletal dysplasia using 3-dimensional computed tomography: a prospective study.

Authors:  Miyoko Waratani; Fumitake Ito; Yukiko Tanaka; Aki Mabuchi; Taisuke Mori; Jo Kitawaki
Journal:  BMC Musculoskelet Disord       Date:  2020-10-08       Impact factor: 2.362

5.  Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report.

Authors:  Fatemeh Rajabi; Ali Hosseini Bereshneh; Mahboubeh Ramezanzadeh; Masoud Garshasbi
Journal:  BMC Pediatr       Date:  2022-01-26       Impact factor: 2.125

Review 6.  Chondrodysplasias With Multiple Dislocations Caused by Defects in Glycosaminoglycan Synthesis.

Authors:  Johanne Dubail; Valérie Cormier-Daire
Journal:  Front Genet       Date:  2021-06-16       Impact factor: 4.599

  6 in total

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