Crouzon, O. (1912) Dysostose cranio-faciale héréditaire. Bulletins et Mémoires de la Société Médicale des Hôpitaux de Paris, 33, 545-555.

has been cited by the following article:

• TITLE: Early Ophthalmological Manifestations of Crouzon Syndrome: About a Case

  AUTHORS: Nidain Maneh, Meba Banla, Nadiedjoa Kokou Douti, Komi Yayehd, Sophie Arsene, Kokou Vonor, Kassoula Batomaguela Nonon Saa, Koffi Didier Ayena, Komi Patrice Balo

  KEYWORDS: Craniofacial Dysostosis

  JOURNAL NAME: Open Access Library Journal, Vol.1 No.7, October 30, 2014

  ABSTRACT: We report the case of a major neonatal form of Crouzon syndrome of ophthalmic finding in a new-born of 21 days of age with no background of consanguinity. The clinical manifestations were marked by signs of Crouzon syndrome associated with dyspnea. The skull radiograph showed a decline of maxillary and closing sutures. The brain scan was marked by a bilateral fronto-parietal hypotrophy with agnenesis of the left temporal. She had received a lateral tarsorrhaphy in prevention to keratopathy of exposure. We noted a substantive consideration of normal eye and no recurrence throttle of eyeball 6 months after tarsorrhaphy. The major forms of Crouzon syndrome is a source of complications including exposure keratopathy and optic atrophy requiring ophthalmological caring in awaiting for a craniofacial surgery.