Literature DB >> 14679586

Desbuquois dysplasia, a reevaluation with abnormal and "normal" hands: radiographic manifestations.

Laurence Faivre1, Valérie Cormier-Daire, Alison M Eliott, Fiona Field, Arnold Munnich, Pierre Maroteaux, Martine Le Merrer, Ralph Lachman.   

Abstract

Radiological features of 35 patients with the diagnosis of Desbuquois dysplasia were analyzed. The diagnosis of Desbuquois dysplasia was based on the association of specific facial alterations, markedly short stature of prenatal onset, joint laxity, "Swedish key" appearance of the proximal femur, and advanced carpal and tarsal bone age. Patients were divided into two groups, depending on whether or not typical hands with an extra ossification center distal to the second metacarpal and/or a delta phalanx of the thumb were present (group 1, 46%) or absent (group 2, 54%). In this study, beside the "Swedish key" appearance of the proximal femur and advanced carpal and tarsal ossification, we were able to define three additional major radiographic criteria for the diagnosis of Desbuquois dysplasia, including flat acetabular roof, elevated greater trochanter, and proximal fibular overgrowth. Other manifestations included wide metaphyses, flat epiphyses, coxa valga, coronal and sagittal clefts of the vertebrae, wide anterior rib portions, medial deviation of the foot, and enlarged first metatarsal. We conclude that characteristic hand abnormalities are not mandatory for the diagnosis of Desbuquois dysplasia. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14679586     DOI: 10.1002/ajmg.a.20440

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


  15 in total

1.  Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2.

Authors:  Long Guo; Nursel H Elcioglu; Aritoshi Iida; Yasemin K Demirkol; Seda Aras; Naomichi Matsumoto; Gen Nishimura; Noriko Miyake; Shiro Ikegawa
Journal:  J Hum Genet       Date:  2016-11-24       Impact factor: 3.172

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 newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delay.

Authors:  Wagner A R Baratela; Michael B Bober; George E Tiller; Ericka Okenfuss; Colleen Ditro; Angela Duker; Deborah Krakow; Deborah L Stabley; Katia Sol-Church; William Mackenzie; Ralph Lachman; Charles I Scott
Journal:  Am J Med Genet A       Date:  2012-06-18       Impact factor: 2.802

4.  MED resulting from recessively inherited mutations in the gene encoding calcium-activated nucleotidase CANT1.

Authors:  Karthika Balasubramanian; Bing Li; Deborah Krakow; Lisette Nevarez; Patric J Ho; Julia A Ainsworth; Deborah A Nickerson; Michael J Bamshad; LaDonna Immken; Ralph S Lachman; Daniel H Cohn
Journal:  Am J Med Genet A       Date:  2017-07-25       Impact factor: 2.802

5.  Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPP.

Authors:  Lisenka E L M Vissers; Ekkehart Lausch; Sheila Unger; Ana Belinda Campos-Xavier; Christian Gilissen; Antonio Rossi; Marisol Del Rosario; Hanka Venselaar; Ute Knoll; Sheela Nampoothiri; Mohandas Nair; Jürgen Spranger; Han G Brunner; Luisa Bonafé; Joris A Veltman; Bernhard Zabel; Andrea Superti-Furga
Journal:  Am J Hum Genet       Date:  2011-05-05       Impact factor: 11.025

6.  XYLT1 mutations in Desbuquois dysplasia type 2.

Authors:  Catherine Bui; Céline Huber; Beyhan Tuysuz; Yasemin Alanay; Christine Bole-Feysot; Jules G Leroy; Geert Mortier; Patrick Nitschke; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2014-02-27       Impact factor: 11.025

7.  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

8.  Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiency.

Authors:  Aleksander Jamsheer; Ewelina M Olech; Kazimierz Kozłowski; Marek Niedziela; Anna Sowińska-Seidler; Monika Obara-Moszyńska; Anna Latos-Bieleńska; Marek Karczewski; Tomasz Zemojtel
Journal:  J Hum Genet       Date:  2016-03-31       Impact factor: 3.172

9.  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

10.  Advanced ossification of the carpal bones, and monkey wrench appearance of the femora, features suggestive of a propable mild form of desbeqious dysplasia: a case report and review of the literature.

Authors:  Ali Al Kaissi; Christof Radler; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2009-01-13
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