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Ariyo, I.J., Mchaile, D.N., Magwizi, M., Kayuza, M., Mrindoko, P. and Chussi, D.C. (2022) Alobar Holoprosencephaly with Cebocephaly in a Neonate: A Rare Case Report from Northern Tanzania. International Journal of Surgery Case Reports, 93, Article ID: 106960.
https://doi.org/10.1016/j.ijscr.2022.106960

has been cited by the following article:

• TITLE: Alobar Holoprosencephaly in a Neonate: A Rare Case Report and Review of the Literature

  AUTHORS: Hanae Bahari, Hanane Hajaj, Anass Ayyad, Sahar Messaoudi, Rim Amrani

  KEYWORDS: Polymalformative Syndrome, Holoprosencephaly, Hydrocephalus

  JOURNAL NAME: Open Journal of Pediatrics, Vol.13 No.6, November 28, 2023

  ABSTRACT: Holoprosencephaly (HPE) is a rare brain malformation with multiple etiologies and is often associated with suggestive facial anomalies. This pathology is the result of a defect in the early development of the forebrain. There are three clinical forms: lobar, semi-lobar, alobar and another milder subtype of HPE called middle interhemispheric. In this clinical case, we present a newborn with alobar holoprosencephaly and we highlight the clinical, radiological and progressive clinical aspects of this illness during the neonatal period.