Results 71 to 80 of about 964,594 (174)
, 1993 I. Fuch\u27s Heterochromic Cyclitis, p.1420; II. "Mosaic" Inheritance of Eye Color and Other Traits, p.1436; III. "Status Dysraphicus," p.1437; IV. Marfan\u27s Syndrome, p.1445; V.
Irene E. Loewenfeld, PhD (1921-2009)
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, 2020 Introduction: Parry-Romberg Syndrome is a neurocutaneous disorder, very rare and characterized by progressive facial hemiatrophy, the first clinical sign is facial asymmetry. SPR occurs simultaneously with high frequency with linear scleroderma.
Mejía Escobar, Cinthya Karina +2 more
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Dyke-Davidoff-Masson syndrome: A rare case report
, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties. It is also called as cerebral hemiatrophy.
Parth Singh Meena +3 more
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Cerebral Hemiatrophy: Etiology and Pathology
, 1991 Two types of cerebral hemiatrophy are reported from the Institute of Neuropathology at the University of Giessen, Arndtstrafse ...
J Gordon Millichap
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, 2005 Progressive facial hemiatrophy, also known as Parry-Romberg syndrome (PRS), is characterized by slowly progressive atrophy of one side of the face, primarily involving the subcutaneous tissues and fat.
Adapinar, B, Uysal, S, Korkmaz, CENGİZ
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Experimental study of progressive facial hematrophy: Effects of cervical sympathecty in animals
, 1991 Progressive facial hemiatrophy (Romberg's syndrome) is of unknown cause and uncertain pathogenesis. The main pathogenetic hypotheses are : sympathetic system alterations, localized scleroderma, trigeminal changes, possibly of genetic origin.
Alves, A., Resende, L. A.L., Dal Pai, V.
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Pansclerotic morphea: A male child with hemiatrophy of lower limb
, 2014 Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and subcutaneous tissue. Pansclerotic morphea is a rare atrophying and sclerosing type of morphea. It can follow a comparatively benign course with spontaneous
Chaitali Patra +3 more
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Automatic facial analysis for objective assessment of facial paralysis [PDF]
, 2009 Facial Paralysis is a condition causing decreased movement on one side of the face. A quantitative, objective and reliable assessment system would be an invaluable tool for clinicians treating patients with this condition. This paper presents an approach
McGrenary, Stewart +3 more
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, 2001 The authors report a case of unilateral, stable, localized, and well-circumscribed choriocapillaris atrophy associated with retinal pigment epithelium dispersion and atrophy. The anterior segment was normal.
Renard, G. +5 more
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Late-onset Parry–Romberg syndrome in a patient with newly diagnosed HIV-2 infection
Revista da Sociedade Portuguesa de Dermatologia e VenereologiaSclerodermoid syndromes encompass a wide spectrum of rare diseases, with variable clinical presentation and severity. We present a case of a 31-year-old woman, Fitzpatrick’s phototype V, who presented to our dermatology department with a 5-year history ...
Claúdia Brazão +7 more
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