Results 31 to 40 of about 119,743 (184)
Parry Romberg syndrome with en coup de sabre: A report of a rare case [PDF]
Acta Stomatologica Naissi, 2021 The basis of the problem: Parry Romberg syndrome (PRS) is a rare developmental disorder manifesting as a slow and progressive atrophy of the face which is often unilateral, hence also termed as rpogressivehemifacial atrophy. The extent of the atrophy may
Faizal Asan Mohamed +4 more
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Facial hemiatrophy: Review of literature and a case report
Journal of Indian Academy of Oral Medicine and Radiology, 2011 A case report of hemifacial atrophy is presented in this paper. It is also known as Parry-Romberg syndrome, is an uncommon degenerative and poorly understood condition.
Manisha S Tijare +4 more
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BMC Neurology, 2009 Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with limited scleroderma linearis.
Brzezińska-Wcisło Ligia +2 more
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Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression [PDF]
Journal of Clinical and Diagnostic Research, 2014 Parry–Romberg syndrome (PRS) or progressive hemifacial atrophy is rare, poorly understood condition with an unclear aetiology and characterized by slow and progressive atrophy affecting one side of the face.
Senthil Kumar +4 more
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AN INDICATION FOR TREATMENT IN HEMIFACIAL ATROPHY [PDF]
The Journal of Nervous and Mental Disease, 1892 n ...
openaire +2 more sources
Facial contouring with parascapular free flap: A case series of 22 cases
Indian Journal of Plastic Surgery, 2013 Background: The facial asymmetry correction in complex craniofacial malformations presents a challenging problem for reconstructive surgeons. Progressive hemifacial atrophy (HFA) and hemifacial microsomia (HFM) can manifest in different grades of ...
Guru Dayal Singh Kalra +1 more
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BMC Neurology, 2023 Background Stroke is rarely accompanied with peripheral facial paralysis and supranuclear palsy of the hypoglossal nerve. Both sides of the motor cortex innervate the hypoglossal nucleus; therefore, unilateral lesions of the upper motor neurons rarely ...
Sangil Park +5 more
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Hemifacial atrophy: an unusual cause of enophthalmos [PDF]
British Journal of Ophthalmology, 1990 We report on two cases of enophthalmos, caused by maxillary atrophy, a rarely reported monostotic forme fruste of hemifacial atrophy.
K N, Hakin, C, Yokoyama, J E, Wright
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South African Family Practice, 2011 Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
F.A. Imarhiagbe, A.O. Adeoti
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Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature. [PDF]
Clin Case RepABSTRACT Juvenile scleroderma (JS) is a rare chronic connective tissue disorder characterized by progressive fibrosis of the skin and soft tissues with/without internal organ involvements. Scleroderma manifests itself in both systemic (SSc) and localized (LS) forms.
Miremarati A +4 more
europepmc +2 more sources