A case report of prenatally detected achondrogenesis type II with an occipital cephalocele
Achondrogenesis is a very rare lethal skeletal disorder. Here we describe a case of prenatally diagnosed achondrogenesis type II in a 28 year-old woman at (17+4) wk. She had history of 5 first trimester missed abortions. The couple is consanguineous. Ultrasonography showed extreme micromelia, short...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2017-01-01
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Series: | Asian Pacific Journal of Reproduction |
Subjects: | |
Online Access: | http://www.apjr.net/article.asp?issn=2305-0500;year=2017;volume=6;issue=5;spage=238;epage=240;aulast=Moradi |