Head injury as a trigger of Parry-Romberg syndrome: A case report and review of etiology

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Head injury as a trigger of Parry-Romberg syndrome: A case report and review of etiology

Introduction: this is a case of a patient with the rare entity of Parry-romberg syndrome (Prs) which discuss the etiological association with preceding head trauma as well as the possible therapeutic role of vitamin b12, with a brief review of literature. case report: A 22-year-old female presented with a history of head injury preceding the progressive onset of right-sided facial pain and atro...

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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: A case report and discussion

Parry Romberg syndrome is a rare disorder of unknown etiology, seen most commonly as an asymmetry of the face, rarely affecting the limbs. Trophic malfunction of sympathetic system has been proposed as a cause. The syndrome presents with characteristic skeletal, dental, and soft tissue changes in the affected half of the face, with or without neurological signs and symptoms. Imaging studies som...

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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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Progressive 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 Case Reports and Images in Medicine

سال: 2016

ISSN: 2581-3544

DOI: 10.5348/z09-2016-12-cr-5