Progressive facial hemiatrophy (Parry-Romberg syndrome), a rare cause of temporal lobe epilepsy: Case report

Abstract

Introduction: Parry-Romberg syndrome is also known as progressive hemifacial atrophy. It, which is characterized by a unilateral atrophy of the skin, soft tissue, muscles, and/or bones of the face, is a variant of linear morphea or an independent disorder. It has sporadic neurocutaneous involvement, occasionally it can even involve the central nervous system (CNS). In this condition, facial atrophy may be accompanied by classic linear morphea lesions on the face or elsewhere. Parry-Romberg syndrome is an uncommon disorder, more common in females, usually manifested in the first decade of life, but its etiology remains unknown.Case Report: A woman with 49 years old, seeking neurological care due to epileptic seizures that started 21 years ago. The crises described were mostly focal, with compromised consciousness, symptomatology related to the temporal lobe with automatisms and sensory