Results 11 to 20 of about 1,581 (159)
Autologous fat grafting in a case of Parry-Romberg syndrome: a case report [PDF]
Case Reports in Plastic Surgery & Hand SurgeryProgressive hemifacial atrophy, also known as Parry-Romberg syndrome (PRS), is an uncommon condition that causes slow and progressive unilateral soft-tissue atrophy of the face.
Bhakti Sarda +3 more
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Chronologic Presentation of a Severe Case of Progressive Hemifacial Atrophy (Parry-Romberg Syndrome) with the Loss of an Eye [PDF]
Case Reports in Otolaryngology, 2014 Progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is a slowly advancing degenerative disease that mostly affects the cutaneous, subcutaneous fatty tissue, muscle tissue, and bone structures on one side of the face.
Mesut Kaya +3 more
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Prosthetic rehabilitation of an orbital defect for a patient with hemifacial atrophy [PDF]
The Journal of Indian Prosthodontic Society, 2016 Removal of an eye may be indicated in cases of congenital abnormality, severe trauma, or disease such as an infection, tumor, or malignancy. The disfigurement associated with a loss of an eye is often accompanied with physical problems, psychological ...
Sanath Shetty +3 more
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Clinical Case ReportsParry‐Romberg Syndrome (PRS) is a rare disorder characterized by progressive unilateral facial atrophy, traditionally viewed as a localized scleroderma variant. Its rare coexistence with systemic lupus erythematosus (SLE) and autoimmune thyroiditis (AIT)
Sakib Abrar +4 more
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Progressive hemifacial atrophy: a review. [PDF]
Orphanet J Rare Dis, 2015 Progressive Hemifacial Atrophy (PHA) is an acquired, typically unilateral, facial distortion with unknown etiology. The true incidence of this disorder has not been reported, but it is often regarded as a subtype of localized scleroderma. Historically, a debate existed whether PHA is a form of linear scleroderma, called morphea en coup de sabre (ECDS),
Tolkachjov SN, Patel NG, Tollefson MM.
europepmc +4 more sources
Dermatology Online Journal, 2013 We report the case of a 44-year-old woman with a one-year history of en coup de sabre morphea and progressive hemifacial atrophy with ipsilateral hemifacial neuralgia, migraine, and contralateral neurologic abnormalities. While rare, Parry-Romberg syndrome typically presents in the first or second decade of life; this patient's case is unusual in that ...
Vedvyas, Chetan, Urbanek, Richard W
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Retinal vasculitis the first clue in the diagnosis of progressive hemifacial atrophy [PDF]
European Journal of Rheumatology, 2019 Atefeh Vafa +3 more
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Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature. [PDF]
Clin Case RepABSTRACT 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.
Miremarati A +4 more
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Romanian Journal of Rheumatology, 2016 Parry-Romberg syndrome, which is also known as progressive facial hemiatrophy, is a variant of localized scleroderma. This is a rare condition (OMIM # 141300), characterized by a progressive but self-limited atrophy of the skin and subcutaneous tissue on
Alexis-Virgil Cochino +2 more
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Case of Rapid Progression of Hemiatrophy on the Face: A New Clinical Entity?
Case Reports in Dermatological Medicine, 2015 A lot of diseases, including lupus profundus, morphea, lipodystrophy, and Parry-Romberg syndrome, may manifest progressive hemifacial atrophy. These diseases usually progress slowly and rapid progression of atrophy is extremely rare.
Hisashi Nomura +3 more
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