Miller Syndrome: A Case Report

Chaimae Khodriss; Ahmed Bennis; Fouad Chraibi; Meriem Abdellaoui; Idriss Benatiya Andaloussi1

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Publication Date: 2021/10/15

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.

Keywords: No Keywords Available

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

PDF: https://ijirst.demo4.arinfotech.co/assets/upload/files/IJISRT21SEP742.pdf

REFERENCES

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