Literature DB >> 15824492

Prenatal ultrasonographic diagnosis of rhizomelic chondrodysplasia punctata by detection of rhizomelic shortening and bilateral cataracts.

Mustafa Başbuğ1, Ibrahim Serdar Serin, Bulent Ozçelik, Tamer Guneş, Mustafa Akçakuş, Mehmet Tayyar.   

Abstract

Antenatal sonographic diagnosis of rhizomelic chondrodysplasia punctata depends on recognization of the combination of rhizomelic bone shortening and epiphyseal stippling. This is the only report of prenatal ultrasonographic diagnosis of bilateral cataracts in a fetus with rhizomelic chondrodysplasia punctata (type 1). Also, this is the first report of severe rhizomelic limb shortening, and bilateral cataracts prior to the recognization of epiphyseal stippling. Copyright (c) 2005 S. Karger AG, Basel.

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Year:  2005        PMID: 15824492     DOI: 10.1159/000083899

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  3 in total

1.  MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlation.

Authors:  Ashley J Robinson; Susan Blaser; Ants Toi; David Chitayat; Sophie Pantazi; Sarah Keating; Sandra Viero; Greg Ryan
Journal:  Pediatr Radiol       Date:  2008-07-17

2.  Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from India.

Authors:  S R Phadke; N Gupta; K M Girisha; M Kabra; M Maeda; E Vidal; A Moser; S Steinberg; R D Puri; I C Verma; N Braverman
Journal:  J Appl Genet       Date:  2010       Impact factor: 3.240

3.  A new GNPAT variant of foetal rhizomelic chondrodysplasia punctata.

Authors:  Adalgisa Cordisco; Elisabetta Pelo; Mariarosaria Di Tommaso; Roberto Biagiotti
Journal:  Mol Genet Genomic Med       Date:  2021-06-10       Impact factor: 2.183

  3 in total

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