Parry–Romberg syndrome

Also known as: Progressive hemifacial atrophy

Progressive unilateral facial atrophy.

Medical specialty: Dermatology
Subspecialty: Dermatology / Connective tissue disorders
Sex & age distribution: Male: affected; Female: affected, female predominance; Children: yes, onset in first two decades
Gene(s) involved: None recorded

Etiology & mechanism

Possibly related to localized scleroderma en coup de sabre.

Gene(s) involved (0)

No gene recorded.

Symptoms & signs (6)

enophthalmoshair losshemifacial atrophymigraineseizurestrigeminal neuralgia

SyndromeScope — educational reference. Content is model-generated and not clinically verified; always confirm against OMIM, Orphanet and GeneReviews before clinical use.