Literature DB >> 18328979

Spondylo-epi-metaphyseal dysplasia.

Valérie Cormier-Daire1.   

Abstract

The spondylo-epi-metaphyseal dysplasias (SEMD) are a heterogeneous group of disorders comprising more than 20 distinct entities with differing modes of inheritance, all defined by the combination of vertebral, epiphyseal and metaphyseal abnormalities. The presenting symptom of SEMD patients is usually disproportionate short stature. The diagnosis is either based on the specificity of the skeletal manifestations or on the presence of characteristic extraskeletal features which may appear during the course of the disease, highlighting the importance of follow-up of SEMD patients. The complications are variable but epiphyseal dysplasia is often a predominant feature, and the course of the disease is marked by premature osteoarthritis. A systematic survey of odontoid hypoplasia responsible for atlantoaxial instability with a risk of spinal cord is also required.

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Year:  2008        PMID: 18328979     DOI: 10.1016/j.berh.2007.12.009

Source DB:  PubMed          Journal:  Best Pract Res Clin Rheumatol        ISSN: 1521-6942            Impact factor:   4.098


  9 in total

1.  Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia.

Authors:  Adetutu T Egunsola; Yangjin Bae; Ming-Ming Jiang; David S Liu; Yuqing Chen-Evenson; Terry Bertin; Shan Chen; James T Lu; Lisette Nevarez; Nurit Magal; Annick Raas-Rothschild; Eric C Swindell; Daniel H Cohn; Richard A Gibbs; Philippe M Campeau; Mordechai Shohat; Brendan H Lee
Journal:  J Clin Invest       Date:  2017-03-06       Impact factor: 14.808

2.  Spondyloepimetaphyseal dysplasia, short limb-abnormal calcifications type: progressive radiological findings from fetal age to adolescence.

Authors:  Katya Rozovsky; Jacob Sosna; Martine Le Merrer; Natalia Simanovsky; Benjamin Z Koplewitz; Jacob Bar-Ziv; Valerie Cormier-Daire; Annick Raas-Rothschild
Journal:  Pediatr Radiol       Date:  2011-08-05

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.  DDRGK1 is required for the proper development and maintenance of the growth plate cartilage.

Authors:  Monika Weisz-Hubshman; Adetutu T Egunsula; Brian Dawson; Alexis Castellon; Ming-Ming Jiang; Yuqing Chen-Evenson; Yu Zhiyin; Brendan Lee; Yangjin Bae
Journal:  Hum Mol Genet       Date:  2022-08-23       Impact factor: 5.121

5.  Mutations in DDR2 gene cause SMED with short limbs and abnormal calcifications.

Authors:  Ruth Bargal; Valerie Cormier-Daire; Ziva Ben-Neriah; Martine Le Merrer; Jacob Sosna; Judith Melki; David H Zangen; Sarah F Smithson; Zvi Borochowitz; Ruth Belostotsky; Annick Raas-Rothschild
Journal:  Am J Hum Genet       Date:  2008-12-24       Impact factor: 11.025

6.  Progressive Pseudorheumatoid Dysplasia Misdiagnosed as Seronegative Juvenile Idiopathic Arthritis.

Authors:  Ozgur Taspinar; Fatih Kelesoglu; Yasar Keskin; Murat Uludag
Journal:  Ethiop J Health Sci       Date:  2016-07

7.  Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M).

Authors:  Liza Das; Vandana Dhiman; Wim Van Hul; Anil Bhansali; Yashpal Gogate; Ellen Steenackers; Geert Mortier; Sanjay Kumar Bhadada
Journal:  Bone Rep       Date:  2020-01-11

8.  Identification of variants in ACAN and PAPSS2 leading to spondyloepi(meta)physeal dysplasias in four Chinese families.

Authors:  Yixuan Cao; Xin Guan; Shan Li; Nan Wu; Xiumin Chen; Tao Yang; Bo Yang; Xiuli Zhao
Journal:  Mol Genet Genomic Med       Date:  2022-03-09       Impact factor: 2.473

9.  Exploring and expanding the phenotype and genotype diversity in seven Chinese families with spondylo-epi-metaphyseal dysplasia.

Authors:  Shanshan Lv; Jiao Zhao; Li Liu; Chun Wang; Hua Yue; Hao Zhang; Shanshan Li; Zhenlin Zhang
Journal:  Front Genet       Date:  2022-08-31       Impact factor: 4.772

  9 in total

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