Literature DB >> 1536165

Intrafamilial variability in cleidocranial dysplasia: a three generation family.

D Chitayat1, K A Hodgkinson, E M Azouz.   

Abstract

We present a 3-generation family, ascertained after the birth of a child with cleidocranial dysplasia (CCD). The propositus presented with respiratory distress (due to a narrow thorax) and hypoplasia and discontinuity of both clavicles. The mother, aunt, and grandmother had varied features of the condition. This intrafamilial variation illustrates the need for clinical assessment of family members following the birth of an apparent sporadic case of CCD.

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Year:  1992        PMID: 1536165     DOI: 10.1002/ajmg.1320420307

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


  14 in total

1.  Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.

Authors:  Areeg H El-Gharbawy; Joseph N Peeden; Ralph S Lachman; John M Graham; Stephen R Moore; David L Rimoin
Journal:  Am J Med Genet A       Date:  2010-01       Impact factor: 2.802

2.  Cleidocranial dysplasia: complete clinical, radiological and histological profiles.

Authors:  Ruchieka Vij; Puneet Batra; Hitesh Vij
Journal:  BMJ Case Rep       Date:  2013-03-20

Review 3.  Cleidocranial dysplasia: clinical and molecular genetics.

Authors:  S Mundlos
Journal:  J Med Genet       Date:  1999-03       Impact factor: 6.318

4.  [Immunohistochemical study on collagen I content in the gingiva in cleidocranial dysplasia].

Authors:  Tobias Ach; Uwe Baumert; Christian Morsczeck; Regine Dahse; Torsten Eugen Reichert; Oliver Driemel
Journal:  Mund Kiefer Gesichtschir       Date:  2007-12

5.  The role of periodontal ligament cells in delayed tooth eruption in patients with cleidocranial dysostosis.

Authors:  Stefan Lossdörfer; Bassel Abou Jamra; Birgit Rath-Deschner; Werner Götz; Rami Abou Jamra; Bert Braumann; Andreas Jäger
Journal:  J Orofac Orthop       Date:  2009-12-04       Impact factor: 1.938

6.  Cleidocranial dysplasia.

Authors:  Ramakant Dixit; Kalpana Dixit; A R Paramez
Journal:  Lung India       Date:  2010-07

7.  Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.

Authors:  Ming Ta Michael Lee; Anne Chun-Hui Tsai; Ching-Heng Chou; Feng-Mei Sun; Li-Chen Huang; Pauline Yen; Chyi-Chyang Lin; Chih-Yang Liu; Jer-Yuarn Wu; Yuan-Tsong Chen; Fuu-Jen Tsai
Journal:  Genomic Med       Date:  2008-08-12

8.  A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Authors:  G J Feldman; N H Robin; L A Brueton; E Robertson; E M Thompson; J Siegel-Bartelt; D L Gasser; L C Bailey; E H Zackai; M Muenke
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

9.  Cleidocranial dysplasia syndrome: clinical characteristics and mutation study of a Chinese family.

Authors:  Shengguo Wang; Shu Zhang; Yanmin Wang; Yangxi Chen; Li Zhou
Journal:  Int J Clin Exp Med       Date:  2013-10-25

10.  Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.

Authors:  Taketoshi Yoshida; Hirokazu Kanegane; Motomi Osato; Masatoshi Yanagida; Toshio Miyawaki; Yoshiaki Ito; Katsuya Shigesada
Journal:  Am J Hum Genet       Date:  2002-08-26       Impact factor: 11.025

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