Results 111 to 120 of about 1,012 (146)

Progressive Hemifacial Atrophy

Surgical Clinics of North America, 1977
Twenty-three cases of progressive hemifacial atrophy with their modalities of treatment have been reviewed. The importance of and need for proper planning and a coordinated approach are stressed. Generally, the final result has been highly satisfactory to the patient.
J E Woods
exaly   +3 more sources

Coloboma in Progressive Hemifacial Atrophy

American Journal of Ophthalmology, 1977
Over a seven-year period, a 22-year-old woman developed clinical linear scleroderma with associated ipsilateral coloboma of the upper eyelid, blepharoptosis, enophthalmos, and impairment of extraocular motility. Reconstructive surgery included correction of the enophthalmos by Silastic block implant, closure of the coloboma, and resection of the ...
Byron Smith
exaly   +3 more sources

Microsurgical Dermal-Fat Retransfer for Progressive Hemifacial Atrophy

Journal of Reconstructive Microsurgery, 2005
Although the etiology of progressive hemifacial atrophy, Romberg's disease, is still unknown, it typically manifests during emotionally salient times, such as the period before the age of 20 years. It involves not only the subcutaneous tissue and skin but also the muscles and osteocartilaginous framework later. Treatment for the atrophy is, in general,
Katsumi Tanaka, Hiroki Yano, Akiyoshi Hirano   +2 more
exaly   +3 more sources

A patient’s experience of progressive hemifacial atrophy

Clinical and Experimental Dermatology
Progressive hemifacial atrophy is a rare idiopathic disorder that can have a significant impact on quality of life. In this article, a patient describes his experience of the condition.
Alan D Irvine, Conor Larney, Irvine Alan D   +2 more
exaly   +3 more sources

Progressive hemifacial atrophy: CT findings

RoFo Fortschritte Auf Dem Gebiet Der Rontgenstrahlen Und Der Bildgebenden Verfahren, 1991
J Casselman
exaly   +2 more sources

Progressive Hemifacial Atrophy with Localized Scleroderma

European Neurology, 2008
We describe a patient with localized scleroderma in association with homolateral atrophy of the tongue and marked ipsilateral facial hemiatrophy which was confirmed histologically. CT scan coronal sections of the face showed severe atrophy of the tongue and facial muscles. The EMG studies failed to demonstrate a neurogenic or myogenic process.
E, Tan, N, Kürkçüoğlu, M, Atalağ, A, Gököz, T, Zileli   +4 more
openaire   +2 more sources

Progressive Hemifacial Atrophy with Linear Scleroderma

Pediatric Dermatology, 2005
Abstract:  We describe a 4‐year‐old girl with hemifacial atrophy. She had a linear white‐colored sclerotic plaque on the right submandibular area of skin. Histologic findings of the lesion were consistent with a diagnosis of scleroderma. The relationship between progressive facial hemiatrophy and linear scleroderma are discussed.
Emine, Dervis, Emel, Dervis
openaire   +2 more sources

Progressive Hemifacial Atrophy (Parry-Romberg Disease)

Journal of Pediatric Ophthalmology & Strabismus, 1987
ABSTRACT Hemifacial atrophy (Parry-Romberg syndrome) is characterized by slowly progressive atrophy of one side of the face, primarily involving the subcutaneous tissue and fat. The onset is usually in the first two decades. Ophthalmic involvement is common; the most frequent abnormality is progressive endophthalmos with subsequent changes in
M T, Miller, H, Sloane, M F, Goldberg, J, Grisolano, M, Frenkel, M F, Mafee   +5 more
openaire   +2 more sources