Ehlers–Danlos syndrome and other heritable connective tissue disorders that impact pregnancies can be detected using next-generation DNA sequencing-Reference-Cited by-同舟云学术

Ehlers–Danlos syndrome and other heritable connective tissue disorders that impact pregnancies can be detected using next-generation DNA sequencing

Published:2019-06-27 Issue:3 Volume:300 Page:491-493
ISSN:0932-0067
Container-title:Archives of Gynecology and Obstetrics
language:en
Short-container-title:Arch Gynecol Obstet

Author:

VanderJagt Krystal^ORCID,Butler Merlin G.

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00404-019-05226-5.pdf

Reference22 articles.

1. Parapia LA, Jackson C (2008) Ehlers–Danlos syndrome—a historical review. Br J Haematol 141:32–35

2. Sen P, Butler MG (2018) Classic Ehlers–Danlos syndrome in a son and father with a heart transplant performed in the father. J Pediatr Genet 8(2):69–72

3. Colombi M, Dordoni C, Chiarelli N, Ritelli M (2015) Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/Ehlers–Danlos syndrome hypermobility type compared to other heritable connective tissue disorders. Am J Med Genet C Semin Med Genet 169C(1):6–22

4. Castori M, Morlino S, Dordoni C, Celletti C, Camerota F, Ritelli M, Morrone A, Venturini M, Grammatico P, Colombi M (2012) Gynecologic and obstetric implications of the joint hypermobility syndrome (a. k. a. Ehlers–Danlos syndrome hypermobility type) in 82 Italian patients. Am J Med Genet A 158A(9):2176–2182

5. Karthikeyan A, Venkat-Raman N (2018) Hypermobile Ehlers–Danlos syndrome and pregnancy. Obstet Med 11(3):104–109

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