%0 Journal Article
%T Alobar Holoprosencephaly in a Neonate: A Rare Case Report and Review of the Literature
%A Hanae Bahari
%A Hanane Hajaj
%A Anass Ayyad
%A Sahar Messaoudi
%A Rim Amrani
%J Open Journal of Pediatrics
%P 929-933
%@ 2160-8776
%D 2023
%I Scientific Research Publishing
%R 10.4236/ojped.2023.136102
%X 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.
%K Polymalformative Syndrome
%K Holoprosencephaly
%K Hydrocephalus
%U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=129360