Mysterious Association of Systemic Lupus Erythematosis with Perry Romberg Syndrome

Parry Romberg syndrome (PRS), also referred to as progressive hemifacial atrophy, facial hemiatrophy, or idiopathic was first described by C and M Romberg.1 It manifests in the two decades morphologically normal-born individuals. commonly affects one more dermatomes trigeminal nerve territory. has an early onset of ophthalmic neurological involvement a variable maxillo-facial cardiac involvement. is idiopathic, gradually craniofacial asymmetry, following atrophy subcutaneous tissue, muscles, osseous, cartilaginous structures. Ophthalmic occurs up 35% cases2. Neurological symptoms manifest 15 20% cases3.