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Airway Ultrasound Findings in a Rare Case of Parry–Romberg Syndrome
AirwayParry–Romberg syndrome (PRS) is a rare disorder characterised by progressive hemifacial atrophy, along with various neurological and ophthalmological manifestations.
Bhavna Gupta +3 more
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Demyelinating etiology as a possible cause of Parry–Romberg Syndrome (PP-14) [PDF]
Neurology Letters, 2023 Parry–Romberg syndrome (PRS) is a rare disease that causes hemiatrophy of the face. The pathophysiological mechanisms involved in its etiology are unknown, but several previous reports suggest the involvement of autoimmune factors.
K. Bahrami +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 with Uhthoff’s Phenomena: A Spectrum of Autoimmune Disease?
Case Reports in Immunology, 2019 Parry–Romberg syndrome (PRS) is a rare disorder characterized by unilateral facial atrophy. Currently, the pathogenesis of PRS is poorly understood and no definitive treatment is available.
Samuel Asanad
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Parry-romberg syndrome: about a case
The Pan African Medical Journal, 2017 A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations
Hanane Oummad, Lalla Ouafae Cherkaoui
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Parry-Romberg syndrome: A case report and literature review
Radiology Case ReportsParry-Romberg syndrome (PRS) is a rare neurocutaneous and craniofacial disorder characterized by progressive hemifacial wasting and atrophy that predominantly affects children and young adults, with an estimated prevalence of 1 in 700,000 individuals ...
Praveen K. Sharma +3 more
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A rare case of Parry-Romberg syndrome with restrictive strabismus
Indian Journal of Ophthalmology. Case ReportsParry-Romberg syndrome is a rare disease characterized by slowly progressive atrophy affecting facial subcutaneous tissues, muscles, osteocartilaginous structures, and possible cerebral involvement.
Nikita Sah +4 more
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Progressive hemifacial atrophy in a Chinese patient: A case report. [PDF]
Medicine (Baltimore), 2022 Li R +12 more
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Progressive Hemifacial Atrophy--case report.
Medicina oral, patologia oral y cirugia bucal, 2006 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. The incidence and the cause of this alteration is unknown. A cerebral disturbance of fat metabolism has been proposed as a primary cause.
da Silva Pinheiro,Thiago Pastor +5 more
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Progressive Hemifacial Atrophy with Morphea of Cheek
Journal of Indian Academy of Oral Medicine and Radiology, 2006 Scleroderma is a rare collagen disorder in which fibrosis of skin, subcutaneous tissues and muscles can occur with occasional involvement of bones. Localized scleroderma is a benign condition but can cause significant deformity when it affects the face ...
Ajit Auluck, Keerthilatha M Pai
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