Abstract
Parry-Romberg syndrome, also known as progressive hemifacial atrophy, was first described by Parry in 1825 then Romberg in 1846. It is a poorly understood rare disorder characterized by progressive hemifacial atrophy of the skin, subcutaneous tissue, and sometimes, the underlying structures including muscles, cartilages and bones. A case report of a Saudi female with this rare disorder is presented with a brief review of the literature.
Article Type
Case Report
First Page
317
Last Page
319
Recommended Citation
Al-Khenaizan, Sultan and Al-Watban, Lemmese
(2005)
"Parry-Romberg syndrome. Overlap with linear morphea,"
Saudi Medical Journal: Vol. 26:
Iss.
2, Article 27.
DOI: https://doi.org/10.15537/1658-3175.2843