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AuthorAl-Khawaja, Fatima
AuthorMadut, Mary J.
AuthorAbdo, Gamal
AuthorNoor, Helmi
AuthorAhmed, Badreldeen
Available date2024-05-15T09:51:59Z
Publication Date2020
Publication NameDonald School Journal of Ultrasound in Obstetrics and Gynecology
Identifierhttp://dx.doi.org/10.5005/jp-journals-10009-1629
CitationMadut, M. J., Abdo, G., Noor, H., & Ahmed, B. (2020). Fetal Holoprosencephaly. Donald School Journal of Ultrasound in Obstetrics and Gynecology, 14(2), 164-166.
ISSN0973-614X
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087161611&origin=inward
URIhttp://hdl.handle.net/10576/55045
AbstractHoloprosencephaly is a birth defect that leads to an abnormal brain development where the brain fails to divide into two hemispheres. Possible causes are environmental or genetic factors. Holoprosencephaly can include craniofacial abnormalities in most of the cases. Here we report a case of delayed diagnosis of holoprosencephaly with cyclopia, proboscis, and ethmocephaly.
Languageen
PublisherJaypee Brothers Medical Publishers (P) Ltd
SubjectAntenatal ultrasound
Fetal malformation
Holoprosencephaly
TitleFetal holoprosencephaly
TypeArticle
Pagination164-166
Issue Number2
Volume Number14
ESSN0975-1912
dc.accessType Full Text


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