Síndrome de Parry-Romberg: hemiatrofia facial progresiva. Reporte de Caso.: Síndrome de Parry-Romberg. [PDF]
, 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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Journal of Cosmetic MedicineHemifacial atrophy, including Parry-Romberg syndrome, is a rare, progressive disorder characterized by unilateral loss of facial soft tissue, with or without neurologic and/or ocular manifestations.
Al Farabi Lee Jaafar +2 more
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Parry-romberg syndrome: difficulties of diagnosis and improvement of treatment [PDF]
, 2020 The article described a case of a rare disease – progressive facial hemiatrophy in a patient of the Neurological Department of Poltava Regional Clinical Hospital. We reviewed a literature on the problem, analyzed the etiological factors, pathogenesis and
Таряник, Катерина Анатоліївна +5 more
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Experimental study of progressive facial hematrophy: Effects of cervical sympathecty in animals [PDF]
, 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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Cortical silent period in a patient with focal epilepsy and Parry-Romberg syndrome [PDF]
, 2005 Progressive facial hemiatrophy (PFH), Parry-Romberg syndrome, is a rare disorder frequently associated with epilepsy. We describe a 28-year-old man who had PFH and partial epilepsy that was easily controlled with antiepileptic drugs.
Oguz, Y, Senol, U, Aktekin, B, Aydin, H
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International Journal of Case Reports and Images, 2021 F. Souza +5 more
semanticscholar +1 more source
Revista Ciencias Biomédicas, 2015 Introduction: the progressive hemifacial atrophy or Parry-Romberg syndrome is a rare disease, of slow clinical evolution that generates atrophy of the soft tissues.
Redondo-Bermúdez César +4 more
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Part Five: Pupillary Pathology: Pupillary Signs in Various Diseases, Chapter 41: Ocular and Systemic Diseases Erroneously Attributed to Sympathetic Impairment [PDF]
, 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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Coexistence of Parry-Romberg syndrome with homolateral segmental vitiligo [PDF]
, 2013 Parry-Romberg syndrome or progressive facial hemiatrophy was first described by Caleb Parry in 1825 and Moritz Romberg in 1846. This disorder is characterized by slowly progressing acquired unilateral hemifacial atrophy, which affects subcutaneous ...
Janowska, Marta +3 more
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Lésion du fond d'oeil séquellaire d'un traumatisme obstétrical: à propos d'un cas [Retinal lesion due to an obstetrical traumatism: a case report]. [PDF]
, 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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