Miller Syndrome: A Case Report


Authors : Chaimae Khodriss; Ahmed Bennis; Fouad Chraibi; Meriem Abdellaoui; Idriss Benatiya Andaloussi

Volume/Issue : Volume 6 - 2021, Issue 9 - September

Google Scholar : http://bitly.ws/gu88

DOI : https://bit.ly/3pan02s

Abstract : Miller syndrome, also known as post-axial acrofacial dysostosis, is a rare congenital genetic disorder, characterized by mandibular and malar hypoplasia, and symmetrical post-axial deficits members. The most frequent ophthalmologic involvement is an ectropion of the lower eyelids.

Miller syndrome, also known as post-axial acrofacial dysostosis, is a rare congenital genetic disorder, characterized by mandibular and malar hypoplasia, and symmetrical post-axial deficits members. The most frequent ophthalmologic involvement is an ectropion of the lower eyelids.

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