Literature DB >> 3340435

Acro-mesomelic dysplasia--a new type. Report of two siblings.

L Brahimi1, L Bacha, K Kozlowski, R Massen, M Zenati.   

Abstract

Two siblings who represent a new type of acro-mesomelic dysplasia are reported. The unique pattern of the acro-mesomelic hypoplastic/dysplastic changes allows us to designate them as a new syndrome.

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Year:  1988        PMID： 3340435     DOI： 10.1007/bf02395764

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  3 in total

1.  [Acrodysostosis].

Authors:  P Maroteaux; G Malamut
Journal:  Presse Med       Date:  1968-11-27       Impact factor: 1.228

2.  A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet.

Authors:  M Eiken; J Prag; K E Petersen; H J Kaufmann
Journal:  Eur J Pediatr       Date:  1984-02       Impact factor: 3.183

3.  Acrofacial dysplasia resembling geleophysic dysplasia.

Authors:  J Spranger; E F Gilbert; S Flatz; M Burdelski; H C Kallfelz
Journal:  Am J Med Genet       Date:  1984-11
  3 in total
  1 in total

1.  Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.

Authors:  S G Kant; A Polinkovsky; S Mundlos; B Zabel; R T Thomeer; H M Zonderland; L Shih; A van Haeringen; M L Warman
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025
  1 in total

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