Results 111 to 120 of about 1,581 (159)
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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.
F A, Ofodile, J E, Woods
openaire   +2 more sources

Hemifacial Atrophy With Intracranial Calcification

Pediatric Neurology, 2013
Yuh-Jyh Jong MD, PhD , Tai-Heng Chen MD* Division of Pediatric Neurology, Departments of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan Division of Pediatric Emergency, Departments
Yuh-Jyh, Jong, Tai-Heng, Chen
openaire   +2 more sources

An unusual case of hemifacial atrophy

Oral Surgery, Oral Medicine, Oral Pathology, 1992
A case of hemifacial atrophy in a 10-year-old boy is described. The presentation in this patient is unusual because the lesion is extremely localized, and the abnormalities of teeth in the affected region are more severe than previously recorded. Alternative diagnoses are considered, and the results of a computed tomographic scan with three-dimensional
R A, Whyman   +3 more
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Treatment options in hemifacial atrophy

European Journal of Plastic Surgery, 1986
Forty-seven patients with hemifacial atrophy are presented an the clinical features of the condition discussed. A series of illustrative cases show the variety of treatment used in this condition and the limitation of the available treatments.
I T Jackson, Jackson I T
exaly   +2 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 ...
B, Smith, C, Guberina
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Ocular manifestations and treatment of hemifacial atrophy

Plastic and Reconstructive Surgery, 1979
Enophthalmos, flattening of the maxilla that may progress to inferior orbital rim and floor defects, eyelid atrophy, and slight relative hypotony occurred in patients with hemifacial atrophy. Less common manifestations included pupillary and iris abnormalities, vertical muscle imbalances, and retinal changes. The prognosis for vision was good.
R S, Muchnick, S J, Aston, T D, Rees
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Hemifacial Atrophy

Ophthalmic Plastic & Reconstructive Surgery, 1995
Progressive hemifacial atrophy or Parry Romberg syndrome may present with variable ocular features, the commonest being enophthalmos. We report a mild case in a 62-year-old man who presented with upper eyelid retraction, nocturnal lagophthalmos, and symptoms of corneal exposure. Recession of the levator muscle corrected the lid retraction and abolished
A, Galanopoulos, A A, McNab
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Hemifacial atrophy with bilateral short roots

British Journal of Oral and Maxillofacial Surgery, 2000
We present a case in which the patient had both bilateral shortening of the roots, and hemifacial atrophy. As far as we know, this combination has not been described before.
A N, Colquhoun   +2 more
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Root resorptions in a patient with hemifacial atrophy

Journal of Endodontics, 1994
Hemifacial atrophy (Parry-Romberg syndrome) is a rare but well-recognized condition. The developmental effects on facial and oral structures have been well documented in the literature. However, the etiology of hemifacial atrophy remains unknown. Previous reported alterations in tooth growth and development include delayed tooth eruption, abnormal root
S, Fayad, B, Steffensen
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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   +4 more
openaire   +2 more sources

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