Alobar holoprosencephaly: A case report

Amirshahi, Mehrbanu and Sanagoo, Akram and Salehi, Ashraf and Kerami, Azam and Abdollahimohammad, Abdolghani and Mirshekari, Fatemeh and Naroei, Fereshteh and Mansoorifar, Leila and Mirshekari, Marzeeh and Mirshekari, Leil (2015) Alobar holoprosencephaly: A case report. Journal of Nursing and Midwifery Sciences, 2 (4). pp. 70-74.

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Official URL: http://jnms.mazums.ac.ir/article-1-163-en.html

Abstract

Holoprosencephaly (HPE) is a rare congenital brain malformation associated with multiple midline facial defects. This anomaly is resulted from the failure of diverticulation and cleavage of primitive prosencephalon during weeks 4-8 of gestation. HPE is the most common forebrain developmental anomaly in human with the incidence rate of 0.49-1.2 cases per 10,000-20,000 term births. In this study, we described a case of HPE in a neonate with gestational age of 32 weeks. Antenatal ultrasonographic diagnosis was performed, and the infant was presented with macrocephaly, bilateral microphthalmia, hypotelorism, proboscis and ambiguous genitalia.

Item Type: Article
Uncontrolled Keywords: Holoprosencephaly, Hypotelorism, Pregnancy, Proboscis, Outcome
Depositing User: Unnamed user with email eprints@mazums.ac.ir
Date Deposited: 04 Jan 2018 19:04
Last Modified: 04 Jan 2018 19:04
URI: http://eprints.mazums.ac.ir/id/eprint/696

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