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Abstract: HLA-DRB1*16 / HLA-DQB1*0301 Haplotypes Confer Susceptibility to Parry Romberg Syndrome
Plastic and Reconstructive Surgery, Global Open, 2018 Damian Palafox, MD +4 more
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A Review of Parry-Romberg Syndrome
Journal of the American Academy of Dermatology, 2012Parry-Romberg syndrome, also known as progressive hemifacial atrophy, is a rare disorder characterized by unilateral facial atrophy affecting the skin, subcutaneous tissue, muscles, and sometimes extending to the osteocartilaginous structures. It has been associated with various systemic manifestations, particularly neurologic, ophthalmologic and ...
Ossama Abbas, Nelly Rubeiz
exaly +3 more sources
New Findings in the Parry-Romberg Syndrome: A Case Report
European Journal of Ophthalmology, 2002 PurposeTo describe further findings in the Parry-Romberg syndrome that might contribute towards a better understanding of the disease.DesignCase report.MethodsThe clinical history of a patient with the Parry-Romberg syndrome was studied, and ...
Francesco Bandello, N Rosa, A Sebastiani
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The Indian Journal of Pediatrics, 2006
Parry-Romberg syndrome, which is also called progressive facial hemiatrophy, overlaps with a condition known as linear scleroderma “en coup de sabre”. It is a rare, acquired, neurocutaneous syndrome of unknown aetiology. The principle features are atrophy of the soft tissues, and sometimes the bone, on one half of the face or forehead without facial ...
Sheffali Gulati +2 more
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Parry-Romberg syndrome, which is also called progressive facial hemiatrophy, overlaps with a condition known as linear scleroderma “en coup de sabre”. It is a rare, acquired, neurocutaneous syndrome of unknown aetiology. The principle features are atrophy of the soft tissues, and sometimes the bone, on one half of the face or forehead without facial ...
Sheffali Gulati +2 more
openaire +2 more sources
Orvosi hetilap, 2020
Parry-Romberg syndrome is a rare, slowly progressive, autolimitated disease, characterized by unilateral facial atrophy. It is usually manifested in childhood and young adulthood. Because of the degree of atrophy and the variety of symptoms, the diagnosis, prognosis, and treatment of Parry-Romberg syndrome are a major challenge.
Tímea, Tamás +3 more
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Parry-Romberg syndrome is a rare, slowly progressive, autolimitated disease, characterized by unilateral facial atrophy. It is usually manifested in childhood and young adulthood. Because of the degree of atrophy and the variety of symptoms, the diagnosis, prognosis, and treatment of Parry-Romberg syndrome are a major challenge.
Tímea, Tamás +3 more
openaire +1 more source
Ophthalmological Manifestations of Parry-Romberg Syndrome
Survey of Ophthalmology, 2016Parry-Romberg syndrome is a rare disease characterized by slowly progressive atrophy affecting facial subcutaneous tissues, including the underlying muscles and osteocartilaginous structures. Various periocular, ocular, and neuro-ophthalmological manifestations have been described in Parry-Romberg syndrome.
Claus Cursiefen, Franziska Bucher
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Parry–Romberg Syndrome: Conventional and Advanced MRI Follow-Up in a Boy
Neuroradiology Journal, 2017 We studied a 9-year-old boy, affected with the Parry–Romberg syndrome, during a period of 32 months, by means of clinical evaluations and neuroradiological magnetic resonance imaging.
Maurizio Cariati, Carla Uggetti
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