Dermatology · Dermatology / Connective tissue disorders
Parry–Romberg syndrome
also: Progressive hemifacial atrophy
Progressive unilateral facial atrophy.
- 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
- Alternative names & eponyms
- Progressive hemifacial atrophy
Etiology & mechanism
Possibly related to localized scleroderma en coup de sabre.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (6)
In plain terms, someone with Parry–Romberg syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
3 shared
Parry–Romberg syndrome with neurological involvement
hemifacial atrophy, migraine, seizures
1 shared
Action myoclonus–renal failure syndrome
seizures
1 shared
Alcohol withdrawal syndrome
seizures
1 shared
Alice in Wonderland syndrome
migraine
1 shared
Amniotic fluid embolism syndrome
seizures
1 shared
Angelman syndrome
seizures
1 shared
Barakat syndrome
seizures
1 shared
Borjeson–Forssman–Lehmann syndrome
seizures
1 shared
Cardiofaciocutaneous syndrome
seizures
1 shared
Cerebral folate deficiency syndrome
seizures
Shares genes with
None.
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