Literature DB >> 8897044

Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) in three neonates.

A L Christianson1, P Beighton.   

Abstract

Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) is a rare, recessive skeletal dysplasia previously reported almost exclusively in Afrikaans speaking South Africans. The condition has been well documented in infants and children. We report on three neonates with SEMDJL, whose presentation highlighted the difficulties inherent in the clinical diagnosis of this condition. SEMDJL may be more widespread than previously considered, as evidenced by the recent documentation of a Guatemalan child with the condition.

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Year:  1996        PMID: 8897044

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  2 in total

1.  A hypoplastic atlas and long odontoid process in a girl manifesting phenotypic features resembling spondyloepimetaphyseal dysplasia joint laxity syndrome.

Authors:  Ali Al Kaissi; Farid Ben Chehida; Maher Ben Ghachem; Klaus Klaushofer; Franz Grill
Journal:  Skeletal Radiol       Date:  2008-02-07       Impact factor: 2.199

2.  Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6.

Authors:  Stefano Giuseppe Caraffi; Ilenia Maini; Ivan Ivanovski; Marzia Pollazzon; Sara Giangiobbe; Maurizia Valli; Antonio Rossi; Silvia Sassi; Silvia Faccioli; Maja Di Rocco; Cinzia Magnani; Belinda Campos-Xavier; Sheila Unger; Andrea Superti-Furga; Livia Garavelli
Journal:  Genes (Basel)       Date:  2019-10-12       Impact factor: 4.096

  2 in total

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