Castañeyra-Perdomo, A., González-Marrero, I., González-Toledo, J.M., Hernández-Abad, L.G., Castañeyra-Ruiz, L., Gonzalez-Arnay, E. and Carmona-Calero, E.M. (2019) A Case of Holoprosencephaly and a Little Review. Human Pathology: Case Reports, 15, 29-32.
https://doi.org/10.1016/j.ehpc.2018.10.014

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.