Results 81 to 90 of about 119,743 (184)
Unilateral Retinal Vasculitis as the Presenting Manifestation of Parry-Romberg Syndrome (Progressive Hemifacial Atrophy). [PDF]
Atchison EA, Szewka AJ, Merrill PT.
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Gray matter atrophy rate as a marker of disease progression in AD. [PDF]
Global gray matter (GM) atrophy rates were quantified from magnetic resonance imaging (MRI) over 6- and 12-month intervals in 37 patients with Alzheimer's disease (AD) and 19 controls using: (1) nonlinear registration and integration of Jacobian values ...
Nick C. Fox +11 more
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Use of cell fat mixed with platelet gel in 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 atrophy affecting one side of the face.
CERVELLI, VALERIO, Gentile P.
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BACKGROUND: Progressive hemifacial atrophy, widely referred to as Parry-Romberg syndrome or Romberg's disease, is a rare pathologic process characterized by an acquired, idiopathic, self-limited, unilateral atrophy of the face, variably involving skin ...
L. Vaienti, M. Soresina, A. Menozzi
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Parry-Romberg syndrome in an adolescent: a case report on progressive hemifacial atrophy. [PDF]
Srinivasan R, Joy ST.
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Hemifacial Hyperplasia - A Case Report
Hemifacial hyperplasia is a rare congenital deformity, affecting soft and bony tissues of one half of the face. The etiology of the condition is unknown and no pattern of heredity is described.
Sanjeev N Deshpande, Leena Deshpande
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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.
Anusha Laxman Rangare +3 more
doaj
Pediatric Patients With Progressive Hemifacial Atrophy: Clinical Features, Course, and Treatment
Progressive hemifacial atrophy (PHA) or Parry‐Romberg syndrome is a rare, insidiously progressive disorder that typically presents in childhood and is considered part of the morphea spectrum.
Selma Scheffler‐Mendoza +3 more
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