Philippine Journal of Otolaryngology Head and Neck Surgery, 2019 Objective: To present a case of progressive hemifacial atrophy in a young woman with Parry-Romberg Syndrome and the role of autologous fat transfer to improve her aesthetic appearance and lessen facial asymmetry.
Ma. Nina Kristine Sison +2 more
doaj +1 more source
Parry Romberg syndrome: A rare case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam +3 more
doaj +1 more source
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
doaj
Clinical evaluation of techniques used in the surgical treatment of progressive hemifacial atrophy [PDF]
, 1994 We critically review 13 patients with progressive hemifacial atrophy treated with three basic surgical procedures (free flap transplantation, alloplastic implants, micro-fat injections ‘lipofilling’) and further ancillary techniques.
Gilbert, P.M. (Philip) +5 more
core +2 more sources
Mild Cognitive Impairment as a single sign of brain hemiatrophy in patient with Localized Scleroderma and Parry : Romberg Syndrome [PDF]
, 2016 Neurologic involvement is well recognized in Systemic Scleroderma and increasingly reported in Localized Scleroderma. MRI brain abnormalities are often associated with symptoms such as seizures or headaches. In some cases they may be clinically silent.
Klimiec-Moskal, Elżbieta +1 more
core +4 more sources
Dental and nondental stem cell based regeneration of the craniofacial region: a tissue based approach [PDF]
, 2016 Craniofacial reconstruction may be a necessary treatment for those who have been affected by trauma, disease, or pathological developmental conditions.
Hughes, Declan, Song, Bing
core +3 more sources
Clinical and therapeutic course in head variants of linear morphea in adults: a retrospective review. [PDF]
, 2022 Parry Romberg Syndrome (PRS) and en coup de sabre (ECDS) are head variants of linear morphea with functional and structural implications. This study describes the clinical course, autoimmune co-morbidities, complications, and treatment of adults with PRS/
Fan, Winnie +4 more
core +1 more source
Detection of anti-Borrelia and anti-Babesia antibodies in the serum of children with clinical manifestations and compatible epidemiology with Lyme-Like disease in the State of Mato Grosso do Sul [PDF]
, 2008 A ocorrência de manifestações clínicas e laboratoriais semelhantes às encontradas na doença de Lyme e da coinfecção com a babesiose já foi demonstrada em trabalhos anteriores em adultos, porém não existem estudos desta natureza em crianças.
ARÃO, César Augusto Brandão +4 more
core +3 more sources
Dyke‐Davidoff‐Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Wasfa Shafiq +7 more
wiley +1 more source
Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT 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.
Aye Miremarati +4 more
wiley +1 more source