Literature DB >> 8255648

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

A Baxova1, K Kozlowski, I Netriova.   

Abstract

A 12.5-year-old girl with severe micromelic dwarfism and characteristic radiographic findings is reported. The most important phenotypic abnormality was dwarfism (stature < 100 cm); the patient had a normal face and intelligence. The diagnostic radiographic findings were those of spondylo-epimetaphyseal dysplasia characterized by severe shortening of humerus, femur and tibia, hypoplastic but normal-shaped fibula, ulna and radius, uniform shortening of the short tubular bones and moderately severe platyspondyly. These radiographic changes were already present at birth, which should make it possible to recognize the disease in the newborn. We propose naming this disorder micromelic dwarfism-humerus, femur, tibia type.

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Year:  1993        PMID: 8255648     DOI: 10.1007/bf02012447

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


  7 in total

1.  Severe dwarfism with cataracts. A new osteo-chondrodysplasia.

Authors:  S Chapman; S Bundey; R F Fletcher
Journal:  Br J Radiol       Date:  1990-12       Impact factor: 3.039

2.  Heterogeneity of nonlethal severe short-limbed dwarfism.

Authors:  G Romeo; J Zonana; D L Rimoin; R S Lachman; C I Scott; E G Kaveggia; J W Spranger; J M Opitz
Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

3.  Dysplasia spondylo-epiphysealis congenita Spranger-Wiedemann. A critical analysis.

Authors:  K Kozlowski; J Masel; K Nolte
Journal:  Australas Radiol       Date:  1977-09

4.  Metatropic dwarfism and its variants.

Authors:  K Kozlowski; L Morris; H Reinwein; P Sprague; L A Tamaela
Journal:  Australas Radiol       Date:  1976-12

5.  [Chondrodysplasia punctata (Chondrodystrophia calcificans) II. The rhizomelic type].

Authors:  J W Spranger; U Bidder; C Voelz
Journal:  Fortschr Geb Rontgenstr Nuklearmed       Date:  1971-03

Review 6.  Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.

Authors:  F Majewski; T Goecke
Journal:  Am J Med Genet       Date:  1982-05

7.  Spondylometepiphyseal dysplasia congenita, Strudwick type.

Authors:  S M Shebib; A E Chudley; M H Reed
Journal:  Pediatr Radiol       Date:  1991
  7 in total

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