Literature DB >> 1903587

Osteochondrodysplasia in Fryns syndrome.

M M Kershisnik1, C M Craven, A L Jung, J C Carey, A S Knisely.   

Abstract

Various skeletal abnormalities have been identified in roentgenograms of persons with Fryns syndrome, but to our knowledge, no histopathologic description of bone or cartilage has been published. We describe disordered endochondral and intramembranous bone formation in a premature female infant with Fryns syndrome. This infant and a full sibling (ie, had same set of parents) with Fryns syndrome in addition exhibited delayed ossification of the basiocciput and of cervical vertebral bodies, also previously undescribed in Fryns syndrome. These findings expand the spectrum of Fryns syndrome to include osteochondrodysplasia.

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Year:  1991        PMID: 1903587     DOI: 10.1001/archpedi.1991.02160060074024

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  2 in total

1.  Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.

Authors:  S Kantarci; D Casavant; C Lee; V Kimonis; B R Pober; C Prada; M Russell; J Byrne; L Wilkins Haug; R Jennings; S Manning; T K Boyd; J P Fryns; L B Holmes; P K Donahoe
Journal:  Am J Med Genet A       Date:  2006-01-01       Impact factor: 2.802

2.  Fryns syndrome: a case associated with karyotype XO.

Authors:  Nader M H Dawani; Abdul Raoof Al Madhoob; Fuad Abdulla Ali; Fatima Shabib
Journal:  Ann Saudi Med       Date:  2004 Mar-Apr       Impact factor: 1.526

  2 in total

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