Parry–Romberg syndrome with neurological involvement

Also known as: Progressive hemifacial atrophy

Progressive facial atrophy.

Medical specialty: Neurology
Subspecialty: Neurology / Neurocutaneous; Rheumatology
Sex & age distribution: Male: affected; Female: affected, more common; Children: yes, onset in first two decades
Gene(s) involved: None recorded

Etiology & mechanism

Unknown; possibly autoimmune.

Gene(s) involved (0)

No gene recorded.

Symptoms & signs (3)

hemifacial atrophymigraineseizures

Note

Neurologic involvement not defining; verify

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