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Amniotic band sequence in paternal half-siblings with vascular Ehlers-Danlos syndrome.

Authors :
Callaghan MB
Hadden R
King JS
Lachlan K
van Dijk FS
Turnpenny PD
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Mar; Vol. 182 (3), pp. 553-556. Date of Electronic Publication: 2019 Dec 12.
Publication Year :
2020

Abstract

Familial amniotic band sequence (ABS) is rare but has been reported in the offspring of mothers with connective tissue disorders. We present a family of two half-siblings with ABS who share the same biological father. Following a serious vascular event a de novo pathogenic variant in COL3A1 was detected in the father, confirming a diagnosis of vascular Ehlers-Danlos syndrome (vEDS). The same variant was found in both his ABS-affected children but not in his unaffected child. The amniotic membrane is derived from fetal tissue, type III collagen being a component. As the affected children are paternal half-siblings, ABS was less likely due to maternal factors. Rather, the amniotic bands may have resulted from decreased type III collagen production as seen in people with vEDS, causing fragility of the amniotic membrane. Consequently, it is important to consider vEDS in patients with ABS.<br /> (© 2019 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1552-4833
Volume :
182
Issue :
3
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
31833208
Full Text :
https://doi.org/10.1002/ajmg.a.61449