Literature DB >> 3793102

Severe short-limb dwarfism resembling Grebe chondrodysplasia.

A S Teebi, S A Al-Awadi, J M Opitz, J Spranger.   

Abstract

A severe, nonlethal short-limb bone dysplasia is described in two unrelated patients. The disorder is characterized by a peculiar facial appearance, rib anomalies and severe shortness and distortion of individual long bones, notably the humeri, tibiae, fibulae, metapodia and phalanges with marked irregularity and asymmetry of bone changes. The condition is differentiated from other bone dysplasias with extreme limb shortness, in particular Grebe chondrodysplasia.

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Year:  1986        PMID: 3793102     DOI: 10.1007/bf00280491

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  12 in total

1.  Nonlethal achondrogenesis (Grebe-Quelce-Salgado type) in two Puerto Rican sibships.

Authors:  J M García-tcastro; A Pérez-Comas
Journal:  J Pediatr       Date:  1975-12       Impact factor: 4.406

2.  A NEW TYPE OF DWARFISM WITH VARIOUS BONE APLASIAS AND HYPOPLASIAS OF THE EXTREMITIES.

Authors:  A QUELCE-SALGADO
Journal:  Acta Genet Stat Med       Date:  1964

3.  Mesomelic skeletal dysplasias.

Authors:  I Kaitila; J T Leisti; D L Rimoin
Journal:  Clin Orthop Relat Res       Date:  1976 Jan-Feb       Impact factor: 4.176

4.  Grebe chondrodysplasia and similar forms of severe short-limbed dwarfism.

Authors:  G Romeo; J Zonana; R S Lachman; J M Opitz; C I Scott; J W Spranger; D L Rimoin
Journal:  Birth Defects Orig Artic Ser       Date:  1977

5.  Pattern recognition in bone dysplasias.

Authors:  J Spranger
Journal:  Prog Clin Biol Res       Date:  1985

6.  [Acromesomelic dwarfism].

Authors:  P Maroteaux; B Martinelli; E Campailla
Journal:  Presse Med       Date:  1971-10-09       Impact factor: 1.228

7.  Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.

Authors:  A G Hunter; M W Thompson
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

8.  Grebe chondrodysplasia and brachydactyly in a family.

Authors:  D Kumar; D Curtis; C E Blank
Journal:  Clin Genet       Date:  1984-01       Impact factor: 4.438

9.  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

10.  [Study of the classification of chondrodysplasias with mesomelic predominance].

Authors:  P Maroteaux; J Spranger
Journal:  Arch Fr Pediatr       Date:  1977-12
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  2 in total

Review 1.  Autosomal recessive disorders among Arabs: an overview from Kuwait.

Authors:  A S Teebi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

2.  Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5.

Authors:  Muhammad Faiyaz-Ul-Haque; Eissa A Faqeih; Hamad Al-Zaidan; Amal Al-Shammary; Syed H E Zaidi
Journal:  J Bone Miner Metab       Date:  2008-11-01       Impact factor: 2.626

  2 in total

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