Parry Romberg syndrome with a wide range of ocular manifestations: a case report

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Parry Romberg syndrome with a wide range of ocular manifestations: a case report

BACKGROUND Parry-Romberg syndrome (PRS) is a rare disorder characterized by unilateral facial atrophy affecting the skin, subcutaneous tissue, muscles, and sometimes extending to the osteocartilaginous structures. Ocular involvement is relatively rare. CASE PRESENTATION We present a case of a 23-year-old female caucasian patient with Parry Romberg syndrome and extensive ocular involvement: en...

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Parry-Romberg Syndrome: a Rare Case Report

BACKGROUND The purpose of this report is to present a rare entity of Parry-Romberg syndrome. This poorly understood degenerative condition is characterised by atrophic changes affecting one side of the face. The cause of these changes remains obscure. METHODS The authors report one rare case of a 31 year old female patient with Parry-Romberg syndrome, accompanied by a brief review of literatu...

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Parry Romberg syndrome with localized scleroderma: A case report

Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome remains unclear. Apart from the multifactorial etiology proposed, the possible primary cause is mainly attributed to the cerebral disturbance ...

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Neurological Manifestations in Parry–Romberg Syndrome: 2 Case Reports

Parry-Romberg syndrome (PRS) is a variant of morphea usually characterized by a slowly progressive course. Clinical and radiological involvement of the central nervous system may be observed in PRS. We describe 2 patients with PRS and neurological symptoms (one with trigeminal neuralgia associated with deafness, and the second with hemifacial pain associated with migraine without aura) in conju...

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Parry-romberg syndrome: about a case

A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations show normal blood counts and rheumatoid factor and antinuclear antibody were negative. CT scan of brain was normal. Fundus examination reveale...

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ژورنال

عنوان ژورنال: BMC Ophthalmology

سال: 2015

ISSN: 1471-2415

DOI: 10.1186/s12886-015-0093-0