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Article

Genetic variations in patient with Parry-Romberg syndrome.

Scientific reports - 9 Jan 2023

Yu Bao-Fu, Dong Li-Ping, Dai Chuan-Chang, Wei Jiao

Abstract excerpt

Parry-Romberg syndrome is a rare craniofacial disorder which is characterized by progressive facial atrophy. The etiology and pathogenesis of the disease are not known. Herein, we report the genetic variants in patient with this disease. A 25-year-old woman was diagnosed with Parry-Romberg syndrome according to her clinical manifestation, which presented with typical progressive unilateral facial soft tissue...

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Identifiers

PMID: 36624141
DOI: 10.1038/s41598-023-27597-1
PMCID: PMC9829853

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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