Parry-Romberg syndrome with multiple intracranial cysts: A rare case report
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چکیده
منابع مشابه
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(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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A giant intracranial aneurysm was diagnosed in a 10-year-old girl when she developed a right abducens nerve palsy. The aneurysm was treated successfully. Six years later, however, she presented with a progressive en coup de sabre deformity, leading to the diagnosis Parry Romberg Syndrome (PRS), a rare diagnosis characterized by hemifacial atrophy of skin, subcutaneous tissue, skeletal muscle an...
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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...
متن کاملProgressive Facial Hemiatrophy. (parry--romberg Syndrome). (a Case Report).
Progressive facial hemiatrophy or Parry-Romberg Syndrome is a rare disease characterized by atrophy in subcutaneous tissues on skin on one half of the face and some accompanied systematic findings. Generally, it develops before the age of 20. It is quite difficult to discriminate it from linear scleroderma localized in fronto-parietal area as they have similar clinical characteristics. In this ...
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ژورنال
عنوان ژورنال: Journal of Pediatric Neurosciences
سال: 2016
ISSN: 1817-1745
DOI: 10.4103/1817-1745.187645