A case report describing insights into the imaging of Apert syndrome

Apert syndrome is a rare congenital autosomal dominant acrocephalosyndactyly type I syndrome which manifests in the form of various craniofacial, skeletal, and visceral anomalies. The present case reports this rare entity in a 15-month-old who presented with multiple craniofacial abnormalities, cran...

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Bibliographic Details
Main Authors: Diksha Goyal, Poonam Sherwani
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Rare
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2950008724000061
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