Literature DB >> 15887273

Autosomal dominant inheritance of spondyloenchondrodysplasia.

R Bhargava1, N J Leonard, A K J Chan, J Spranger.   

Abstract

Spondyloenchondrodysplasia comprises generalized enchondromatosis with platyspondyly and is thought to be inherited as an autosomal recessive condition. A mother and son are reported with typical features of spondyloenchondrodysplasia. Their similar radiographic and MRI findings are presented. The radiologic appearance of the spine changed over time, illustrating the evolving phenotype of this condition. Transmission from mother to son suggests that dominant pattern of inheritance is possible. A classification of the enchondromatoses is discussed.

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Mesh:

Year:  2005        PMID: 15887273     DOI: 10.1002/ajmg.a.30732

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


  6 in total

1.  Common somatic alterations identified in maffucci syndrome by molecular karyotyping.

Authors:  Mustapha Amyere; Anne Dompmartin; Vinciane Wouters; Odile Enjolras; Ilkka Kaitila; Pierre-Louis Docquier; Catherine Godfraind; John Butler Mulliken; Laurence Myriam Boon; Miikka Vikkula
Journal:  Mol Syndromol       Date:  2014-08-26

2.  Dysmorphic facies and diffuse posterior spine ankylosis in a patient with unusual form of spondyloenchondrodysplasia (Spranger type IV).

Authors:  Ali Al Kaissi; Farid Ben Chehida; Maher Ben Ghachem; Klaus Klaushofer; Franz Grill
Journal:  Eur Spine J       Date:  2012-09-30       Impact factor: 3.134

Review 3.  Enchondromatosis: insights on the different subtypes.

Authors:  Twinkal C Pansuriya; Herman M Kroon; Judith V M G Bovée
Journal:  Int J Clin Exp Pathol       Date:  2010-06-26

4.  A Case with Spondyloenchondrodysplasia Treated with Growth Hormone.

Authors:  Takanori Utsumi; Satoshi Okada; Kazushi Izawa; Yoshitaka Honda; Gen Nishimura; Ryuta Nishikomori; Rika Okano; Masao Kobayashi
Journal:  Front Endocrinol (Lausanne)       Date:  2017-07-10       Impact factor: 5.555

5.  Craniofacial anomalies associated with spondyloenchondrodysplasia: Two case reports.

Authors:  Seok Woo Hong; Kyung-Hoe Huh; Jeong Keun Lee; Jeong-Hyun Kang
Journal:  Medicine (Baltimore)       Date:  2018-12       Impact factor: 1.817

6.  Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey.

Authors:  Tracy A Briggs; Gillian I Rice; Navid Adib; Lesley Ades; Stephane Barete; Kannan Baskar; Veronique Baudouin; Ayse N Cebeci; Philippe Clapuyt; David Coman; Lien De Somer; Yael Finezilber; Moshe Frydman; Ayla Guven; Sébastien Heritier; Daniela Karall; Muralidhar L Kulkarni; Pierre Lebon; David Levitt; Martine Le Merrer; Agnes Linglart; John H Livingston; Vincent Navarro; Ericka Okenfuss; Anne Puel; Nicole Revencu; Sabine Scholl-Bürgi; Marina Vivarelli; Carine Wouters; Brigitte Bader-Meunier; Yanick J Crow
Journal:  J Clin Immunol       Date:  2016-03-08       Impact factor: 8.317

  6 in total

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