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Parry–Romberg syndrome

ICD-10: G51.8MeSH: D005150ORPHA: 1214

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with Parry–Romberg syndrome, sourced from HPO and Orphanet clinical annotations.

Abnormal mandible morphologyFacial asymmetryMicrognathiaIrregular hyperpigmentationSeizureAbnormality of the musculatureAplasia/Hypoplasia of the skinAsymmetric growthDeeply set eyePtosisHeterochromia iridis

Classification & Codes

ICD-10 Code

G51.8

MeSH Code

D005150

Orphanet Code

ORPHA:1214
Parry–Romberg syndrome
ICD-10G51.8
MeSHD005150
OrphanetORPHA:1214
Treatments0 drug(s)
Symptoms on record11 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO