Literature DB >> 22791316

Enchondromatosis revisited: new classification with molecular basis.

Andrea Superti-Furga1, Jürgen Spranger, Gen Nishimura.   

Abstract

The so-called "enchondromatoses" are skeletal disorders defined by the presence of ectopic cartilaginous tissue within bone tissue. The clinical and radiographic features of the different enchondromatoses are distinct, and grouping them does not reflect a common pathogenesis but simply a similar radiographic appearance and thus the need for a differential diagnosis. Recent advances in the understanding of their molecular and cellular bases confirm the heterogeneous nature of the different enchondromatoses. Some, like Ollier disease, Maffucci disease, metaphyseal chondromatosis with hydroxyglutaric aciduria, and metachondromatosis are produced by a dysregulation of chondrocyte proliferation, while others (such as spondyloenchondrodysplasia or dysspondyloenchondromatosis) are caused by defects in structure or metabolism of cartilage or bone matrix. In other forms (e.g., the dominantly inherited genochondromatoses), the basic defect remains to be determined. The classification, proposed by Spranger and associates in 1978 and tentatively revised twice, was based on the radiographic appearance, the anatomic sites involved, and the mode of inheritance. The new classification proposed here integrates the molecular genetic advances and delineates phenotypic families based on the molecular defects. Reference radiographs are provided to help in the diagnosis of the well-defined forms. In spite of advances, many cases remain difficult to diagnose and classify, implying that more variants remain to be defined at both the clinical and molecular levels.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22791316     DOI: 10.1002/ajmg.c.31331

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  5 in total

1.  Longitudinal Follow-Up of Two Patients with Dysspondyloenchondromatosis due to Novel Heterozygous Mutations in COL2A1.

Authors:  Nilay Güneş; Gözde Yeşil; Kubilay Beng; Sinan Kahraman; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2018-04-24

2.  Rare diseases in clinical endocrinology: a taxonomic classification system.

Authors:  G Marcucci; L Cianferotti; P Beck-Peccoz; M Capezzone; F Cetani; A Colao; M V Davì; E degli Uberti; S Del Prato; R Elisei; A Faggiano; D Ferone; C Foresta; L Fugazzola; E Ghigo; G Giacchetti; F Giorgino; A Lenzi; P Malandrino; M Mannelli; C Marcocci; L Masi; F Pacini; G Opocher; A Radicioni; M Tonacchera; R Vigneri; M C Zatelli; M L Brandi
Journal:  J Endocrinol Invest       Date:  2014-11-07       Impact factor: 4.256

Review 3.  Monogenic systemic lupus erythematosus: insights in pathophysiology.

Authors:  Ezgi Deniz Batu
Journal:  Rheumatol Int       Date:  2018-05-15       Impact factor: 2.631

4.  FGFR3 Deficiency Causes Multiple Chondroma-like Lesions by Upregulating Hedgehog Signaling.

Authors:  Siru Zhou; Yangli Xie; Junzhou Tang; Junlan Huang; Qizhao Huang; Wei Xu; Zuqiang Wang; Fengtao Luo; Quan Wang; Hangang Chen; Xiaolan Du; Yue Shen; Di Chen; Lin Chen
Journal:  PLoS Genet       Date:  2015-06-19       Impact factor: 5.917

Review 5.  Sclerosing angiomatoid nodular transformation of the spleen in a patient with Maffucci syndrome: a case report and review of literature.

Authors:  Xiao-Dan Huang; Hao-Sen Jiao; Zheng Yang; Chuang-Qi Chen; Yu-Long He; Xin-Hua Zhang
Journal:  Diagn Pathol       Date:  2017-11-10       Impact factor: 2.644

  5 in total

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