Year: 2024
Type: article
Study design: Case Report
Abstract: Parry–Romberg syndrome is a rare cause of hemifacial atrophy with associated other systemic complaints including neurological symptoms. Diagnosis is based on history and clinical examination supported by imaging. Here, we report a case of a 10-year-old female presenting with gradually progressive left hemifacial atrophy for 2 years and describe the clinical and imaging findings of the patient.
Institutions: Institute of Medical Sciences, Banaras Hindu University
Language: English
Subfield: Pathology and Forensic Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
OpenAlex ID: W4402284599
