Mirror movements in progressive hemifacial atrophy
نویسندگان
چکیده
منابع مشابه
Progressive hemifacial atrophy
Progressive hemifacial atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive but self-limited atrophy affecting one side of the face. The incidence and the cause of this alteration are unknown. A cerebral disturbance of fat metabolism has been proposed as a primary cause. Possible factors that ar...
متن کاملprogressive hemifacial atrophy
progressive hemifacial atrophy, also known as parry-romberg syndrome, is an uncommon degenerative and poorly understood condition. it is characterized by a slow and progressive but self-limited atrophy affecting one side of the face. the incidence and the cause of this alteration are unknown. a cerebral disturbance of fat metabolism has been proposed as a primary cause. possible factors that ar...
متن کاملProgressive Hemifacial Atrophy--case report.
Progressive Hemifacial Atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive atrophy affecting one side of the face. The incidence and the cause of this alteration is unknown. A cerebral disturbance of fat metabolism has been proposed as a primary cause. This can be the result of a trophic malfor...
متن کاملProgressive hemifacial atrophy: a review
BACKGROUND Progressive Hemifacial Atrophy (PHA) is an acquired, typically unilateral, facial distortion with unknown etiology. The true incidence of this disorder has not been reported, but it is often regarded as a subtype of localized scleroderma. Historically, a debate existed whether PHA is a form of linear scleroderma, called morphea en coup de sabre (ECDS), or whether these conditions are...
متن کاملProgressive hemifacial atrophy: a case report.
A case of a 28-year-old Caucasian female with progressive hemifacial atrophy and atrophy of the rhomboid muscles on the ipsilateral side is reported. The literature on this condition and its treatment is reviewed.
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ژورنال
عنوان ژورنال: Annals of Indian Academy of Neurology
سال: 2015
ISSN: 0972-2327
DOI: 10.4103/0972-2327.150606