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.
View as HTML
