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Dermatosparaxis (Ehlers-Danlos type VIIC): prenatal diagnosis following a previous pregnancy with unexpected skull fractures at delivery.

Authors :
Solomons J
Coucke P
Symoens S
Cohen MC
Pope FM
Wagner BE
Sobey G
Black R
Cilliers D
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2013 May; Vol. 161A (5), pp. 1122-5. Date of Electronic Publication: 2013 Mar 13.
Publication Year :
2013

Abstract

Dermatosparaxis Ehlers-Danlos syndrome (or EDS VIIC), a rare autosomal recessive connective tissue disorder, is characterized by extreme skin fragility, premature rupture of membranes in pregnancy, and spontaneous rupture of internal organs. Here we report a second patient with EDS VIIC presenting with congenital skull fractures and skin lacerations at birth, complications which may occur more frequently than previously thought in this condition. We also discuss the role of prenatal diagnosis in the management of a subsequent normal pregnancy.<br /> (Copyright © 2012 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1552-4833
Volume :
161A
Issue :
5
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
23495203
Full Text :
https://doi.org/10.1002/ajmg.a.35802