Familial Parry-Romberg disease

Peter J. Anderson*, Darren Molony, Eric Haan, David J. David

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

Parry-Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members.

Original languageEnglish
Pages (from-to)705-708
Number of pages4
JournalInternational Journal of Pediatric Otorhinolaryngology
Volume69
Issue number5
DOIs
Publication statusPublished - May 2005
Externally publishedYes

Keywords

  • Face
  • Hemifacial atrophy
  • Parry-Romberg disease

Fingerprint

Dive into the research topics of 'Familial Parry-Romberg disease'. Together they form a unique fingerprint.

Cite this