Axenfeld–Rieger Syndrome: A Case Report and Brief Review

Axenfeld–Rieger Syndrome (ARS) is a rare autosomal dominant genetic disorder with an overall incidence of 1:200,000 that has mainly ocular, periumbilical, and dental abnormalities like oligodontia/hypodontia, microdontia, and delayed eruption of permanent teeth. Its management requires a multidiscip...

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Bibliographic Details
Published in:Journal of South Asian Association of Pediatric Dentistry
Main Authors: Amina Sultan, Simran Uppal, Akanksha Juneja
Format: Article
Language:English
Published: Jaypee Brothers Medical Publisher 2024-04-01
Subjects:
axenfeld–rieger syndrome
case report
everted umbilicus
glaucoma
hypodontia
oligodontia
Online Access:https://www.jsaapd.com/doi/JSAAPD/pdf/10.5005/jp-journals-10077-3291

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https://www.jsaapd.com/doi/JSAAPD/pdf/10.5005/jp-journals-10077-3291

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