Literature DB >> 925797

Heterogeneity of nonlethal severe short-limbed dwarfism.

G Romeo, J Zonana, D L Rimoin, R S Lachman, C I Scott, E G Kaveggia, J W Spranger, J M Opitz.   

Abstract

The Grebe syndrome is a nonlethal form of severe short-limbed dwarfism which was previously called "achondrogenesis-Brazilian or Grebe type". We have studied three patients with severe short-limbed dwarfism originally considered to have this syndrome. On re-evaluation of their clinical and radiographic features, only one of them had the typical features of the Grebe chondrodysplasia, whereas the other two appear to have clearly distinct, previously unreported skeletal dysplasias. These patients illustrate the heterogeneity that exists among the nonlethal forms of severe short-limbed dwarfism.

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Year:  1977        PMID: 925797     DOI: 10.1016/s0022-3476(77)80890-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  3 in total

1.  A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.

Authors:  L O Langer; J Cervenka; M Camargo
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

2.  Severe short-limb dwarfism resembling Grebe chondrodysplasia.

Authors:  A S Teebi; S A Al-Awadi; J M Opitz; J Spranger
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

3.  Micromelic dwarfism--humerus, femur, tibia type. Report of a case.

Authors:  A Baxova; K Kozlowski; I Netriova
Journal:  Pediatr Radiol       Date:  1993
  3 in total

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