Stellate ganglion block and de-epithelialized free flap transfer in a patient with progressive hemifacial atrophy.

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Progressive 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...

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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...

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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...

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Adipofascial anterolateral thigh free flap for hemifacial atrophy.

Restoration of a harmonious and pleasant appearance is a crucial aspect of surgical treatment for many congenital and acquired deformities of the face. A 38-year-old female patient with residual scarring on the right hemiface following evacuation of a odontogenic phlegmon underwent microsurgical reconstruction with a free adipofascial anterolateral thigh free flap. A stable result was achieved ...

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progressive hemifacial atrophy with contralateral uveitis: a case report

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ژورنال

عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery

سال: 1998

ISSN: 2186-1579,0021-5163

DOI: 10.5794/jjoms.44.753