Literature DB >> 3041395

Cardiovascular pathology in osteogenesis imperfecta type IIA with a review of the literature.

V R Wheeler1, N R Cooley, W R Blackburn.   

Abstract

Lethal perinatal osteogenesis imperfecta (OI Type II) is a biochemically diverse collagen disorder characterized by short, crumpled long bones, beaded ribs, blue sclerae and thin, fragile skin. Cardiovascular abnormalities are rarely described. Using morphometry and light and electron (SEM and TEM) microscopy, we analyzed the hearts and great vessels from 2 fetuses with OI Type IIA and compared the findings with age-matched controls. The heart weights and atrioventricular valve (AVV) circumferences were reduced in OI. The chordae tendineae were short and fragile; both the AVVs and the chordae tendineae were hypercellular. TEM showed relatively little organized collagen in the chordae tendineae of OI fetuses. Furthermore, quantitative evaluation of collagen fibril size revealed a decrease in the cross-sectional diameter. There was also a marked decrease in the adventitial and intramural collagen of the intramyocardial arteries and great vessels in OI. Our study reports, for the first time, specific lesions in the cardiovascular systems of patients with OI Type II and reviews the cardiovascular pathology in other forms of OI.

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Year:  1988        PMID: 3041395     DOI: 10.3109/15513818809022279

Source DB:  PubMed          Journal:  Pediatr Pathol        ISSN: 0277-0938


  3 in total

1.  Echocardiographic Evidence of Early Diastolic Dysfunction in Asymptomatic Children with Osteogenesis Imperfecta.

Authors:  Khalfan S Al-Senaidi; Irfan Ullah; Hashim Javad; Murtadha Al-Khabori; Saif Al-Yaarubi
Journal:  Sultan Qaboos Univ Med J       Date:  2015-11-23

2.  Abnormalities in the cerebral arterial system in osteogenesis imperfecta.

Authors:  Sait Albayram; Osman Kizilkilic; Halit Yilmaz; Beyhan Tuysuz; Naci Kocer; Civan Islak
Journal:  AJNR Am J Neuroradiol       Date:  2003-04       Impact factor: 3.825

3.  Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.

Authors:  Frank Thiele; Christian M Cohrs; Armando Flor; Thomas S Lisse; Gerhard K H Przemeck; Marion Horsch; Anja Schrewe; Valerie Gailus-Durner; Boris Ivandic; Hugo A Katus; Wolfgang Wurst; Catherine Reisenberg; Hollis Chaney; Helmut Fuchs; Wolfgang Hans; Johannes Beckers; Joan C Marini; Martin Hrabé de Angelis
Journal:  Hum Mol Genet       Date:  2012-05-15       Impact factor: 6.150

  3 in total

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