Aarskog–Scott syndrome – prenatal ultrasound diagnosis in a case with positive family history

Aarskog–Scott syndrome (AAS), which is also known as faciogenital dysplasia, is a rare developmental disorder inherited mainly as an X-linked recessive trait. Broad hands with brachydactyly, facial clefts, a small nose and an increased upper-to-lower-segment ratio represent the features amenable to...

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Bibliographic Details
Main Authors: Nawal Hubaishi, Fatima Cherifi, Maryam Khalid Taka, Amina Bin Ashoor, Dario Paladini
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Hamdan Medical Journal
Online Access:http://www.hamdanjournal.org/article.asp?issn=2227-2437;year=2017;volume=10;issue=3;spage=187;epage=190;aulast=Hubaishi;type=0