Literature DB >> 2325095

A case of atelosteogenesis.

K Temple1, C A Hall, L Chitty, M Baraitser.   

Abstract

Atelosteogenesis is a rare chondrodysplasia characterised by rhizomelic short limbed dwarfism, thoracic hypoplasia, multiple joint dislocations, talipes equinovarus, and early death. The diagnosis is confirmed radiologically: short, distally tapering humeri, absent or hypoplastic fibulae, deficient vertebral ossification with coronal clefting, and anarchic ossification of phalanges are characteristic findings. We report a male child with this condition born to first cousin Bengali parents.

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Year:  1990        PMID: 2325095      PMCID: PMC1017004          DOI: 10.1136/jmg.27.3.194

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Variant of atelosteogenesis? Report of a 20-week fetus.

Authors:  A J Herzberg; E L Effmann; W D Bradford
Journal:  Am J Med Genet       Date:  1988-04

2.  New forms of neonatal death dwarfism. Report of 3 cases.

Authors:  K Kozlowski; T Tsuruta; Y Kameda; A Kan; G Leslie
Journal:  Pediatr Radiol       Date:  1981-02

3.  Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia.

Authors:  D O Sillence; R S Lachman; T Jenkins; V M Riccardi; D L Rimoin
Journal:  Am J Med Genet       Date:  1982-09

4.  Atelosteogenesis.

Authors:  P Maroteaux; J Spranger; V Stanescu; B Le Marec; R A Pfeiffer; P Beighton; J F Mattei
Journal:  Am J Med Genet       Date:  1982-09

5.  Two lethal chondrodysplasias with giant chondrocytes.

Authors:  S S Yang; J Roskamp; C T Liu; R Frates; D B Singer
Journal:  Am J Med Genet       Date:  1983-08
  5 in total
  3 in total

1.  A new lethal skeletal dysplasia or the severe end of the atelosteogenesis spectrum?

Authors:  A E Fryer; H Carty
Journal:  Pediatr Radiol       Date:  1996-09

Review 2.  Atelosteogenesis type 2.

Authors:  R Newbury-Ecob
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

3.  Identification of a de novo heterozygous missense FLNB mutation in lethal atelosteogenesis type I by exome sequencing.

Authors:  Ga Won Jeon; Mi-Na Lee; Ji Mi Jung; Seong Yeon Hong; Young Nam Kim; Jong Beom Sin; Chang-Seok Ki
Journal:  Ann Lab Med       Date:  2014-02-13       Impact factor: 3.464

  3 in total

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