Literature DB >> 8471223

An unclassifiable type of spondylo-peripheral epiphyseal dysplasia associated with 21 trisomy.

D M Ioan1, M Popa, J P Fryns.   

Abstract

We present an unusual type of skeletal dysplasia in a 6 1/2 year-old female child with Down syndrome due to classical 21 trisomy. Differential diagnosis with the pseudoachrondroplastic forms of spondyloepiphyseal dysplasia shows that the epiphyseal changes in the present patient are unique and do not allow to classify the skeletal changes of the present patient in this group of disorders.

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Year:  1993        PMID: 8471223

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


  1 in total

1.  Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.

Authors:  Yuri A Zarate; Katherine A Bosanko; Elizabeth Bhoj; Rebecca Ganetzky; Lois J Starr; Elaine H Zackai; G Bradley Schaefer
Journal:  Am J Med Genet A       Date:  2015-04-25       Impact factor: 2.802

  1 in total

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