Literature DB >> 6507479

Fibrochondrogenesis: radiologic and histologic studies.

D J Eteson, G E Adomian, A Ornoy, T Koide, Y Sugiura, A Calabro, S Lungarotti, P Mastroiacovo, R S Lachman, D L Rimoin.   

Abstract

Fibrochondrogenesis is a distinct, neonatally lethal, short-limb skeletal dysplasia which was first described in a single patient in 1978. We report the radiographic and morphologic studies of 2 additional unrelated stillborn infants with fibrochondrogenesis. This syndrome has distinct radiographic and chondro-osseous morphologic defects different from those seen in the other known skeletal dysplasias. The long bones are short and dumbbell-shaped with metaphyseal flare. The spine is platyspondylic with superior-inferior clefting defects, and the ribs are short and distally cupped. The growth-plate cartilage is grossly disorganized and has a densely fibrous collagenous matrix when examined by light and electron microscopy. Light, transmission, and scanning electron microscopy shows diaphyseal and metaphyseal trabecular bone to be normal.

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Year:  1984        PMID: 6507479     DOI: 10.1002/ajmg.1320190210

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


  5 in total

1.  Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene.

Authors:  Stuart W Tompson; Carlos A Bacino; Nicole P Safina; Michael B Bober; Virginia K Proud; Tara Funari; Michael F Wangler; Lisette Nevarez; Leena Ala-Kokko; William R Wilcox; David R Eyre; Deborah Krakow; Daniel H Cohn
Journal:  Am J Hum Genet       Date:  2010-10-28       Impact factor: 11.025

2.  A new case of fibrochondrogenesis from Spain.

Authors:  M L Martínez-Frías; A García; J Cuevas; J I Rodríguez; M Urioste
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

3.  Fibrochondrogenesis.

Authors:  M L Kulkarni; Prakash S Matadh; S P Praveen Prabhu; Preeti M Kulkarni
Journal:  Indian J Pediatr       Date:  2005-04       Impact factor: 1.967

4.  Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2.

Authors:  Stuart W Tompson; Eissa Ali Faqeih; Leena Ala-Kokko; Jacqueline T Hecht; Rika Miki; Tara Funari; Vincent A Funari; Lisette Nevarez; Deborah Krakow; Daniel H Cohn
Journal:  Am J Med Genet A       Date:  2012-01-13       Impact factor: 2.802

5.  Metatropic dysplasia lethal variants.

Authors:  Christine M Hall; Nursel H Elçioglu
Journal:  Pediatr Radiol       Date:  2003-10-18
  5 in total

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