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Cuisset, J.M., Cuvellier, J.C., Vallée, L., Ryckewäert, P., Soto-Ares, G. and Nuyts, J.P. (1999) Holoprosencephaly with Neurogenic Hypernatremia. Archives de Pédiatrie, 6, 43-45.
https://doi.org/10.1016/S0929-693X(99)80072-4

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.