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Dermatosparaxis (Ehlers-Danlos type VIIC): prenatal diagnosis following a previous pregnancy with unexpected skull fractures at delivery.
- 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.)
- Subjects :
- ADAMTS4 Protein
Ehlers-Danlos Syndrome complications
Ehlers-Danlos Syndrome genetics
Female
Humans
Infant, Newborn
Microscopy, Electron, Transmission
Pregnancy
ADAM Proteins genetics
Delivery, Obstetric adverse effects
Ehlers-Danlos Syndrome diagnosis
Prenatal Diagnosis methods
Procollagen N-Endopeptidase genetics
Rupture, Spontaneous complications
Skull Fractures complications
Subjects
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