Results 11 to 20 of about 1,700 (192)

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, Ceyda Sel Yilmaz, Hanifi Kurtaran, Mehmet Gunduz   +3 more
doaj   +2 more sources

Progressive hemifacial atrophy : Case report [PDF]

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
Camarinha-da Silva, Camila, da Silva Pinheiro, Thiago Pastor, Ereno Botelho, Patrícia Cristina, Limeira da Silveira, Carolina Souza, Rodrigues Pinheiro, Maria das Graças, Viana Pinheiro, João de Jesus   +5 more
core   +6 more sources

Progressive Hemifacial Atrophy - A Case Report

Journal of Indian Academy of Oral Medicine and Radiology, 2006
Progressive Hemifacial atrophy (Parry-Romberg disease) is a rare condition affecting the face. It commences in childhood but its aetiology and pathogenisis remains unknown, and is sporadic.
Mathew Philip, Prasanth K Shenai, Laxmikanth Chatra   +2 more
doaj   +2 more sources

Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria [PDF]

South African Family Practice, 2011
Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
F.A. Imarhiagbe, A.O. Adeoti
doaj   +3 more sources

Progressive Hemifacial Atrophy With Contralateral Uveitis: A Case Report. [PDF]

Iran Red Crescent Med J, 2015
Progressive hemifacial atrophy, known as Parry-Romberg syndrome (PRS), was first described by Parry in 1825. There is a progressive atrophy of facial tissues including skin, bones and muscles. Ophthalmic disorders are common and include keratitis, uveitis, cataract, ipsilateral enophthalmos, optic neuritis, retinal vasculitis and scleral melting.We ...
Ayyildiz O, Ayyildiz S, Durukan AH, Sobaci G.   +3 more
europepmc   +4 more sources

Treatment of Mild-to-moderate Progressive Hemifacial Atrophy by Acellular Dermal Matrix Combined With Preoperative Digital Evaluation [PDF]

Plastic and Reconstructive Surgery, Global Open
Background:. Progressive hemifacial atrophy (PHA) is a rare condition marked by the gradual degeneration of skin, soft tissues, muscles, and, in advanced stages, bone.
Xinhao Cheng, MS, Haijiang Dong, MD, PhD, Chengxiang Yan, MS, Zhibin Li, MS, Baihui Xie, MS, Yu Li, MD, PhD, Huilong Liu, MS, Yijun Zhang, Ximei Wang, MD, PhD   +8 more
doaj   +2 more sources

Progressive Hemifacial Atrophy (Parry-Romberg Syndrome)

Journal of Indian Academy of Oral Medicine and Radiology
Progressive hemifacial atrophy (PHA), also known as Parry-Romberg syndrome (PRS), is an auto-limitable condition with unknown etiology, characterized by slow and progressive hemiatrophy affecting one side of the face.
Nalini Aswath, Rajalakshmi Rakshanaa
doaj   +2 more sources

A Complex Inflammatory Triad: A Rare Case of Parry‐Romberg Syndrome With Systemic Lupus Erythematosus and Thyroiditis

Clinical Case Reports
Parry‐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, Fabiha Rahman Spriha, Sajjad Ghanim Al‐Badri, Md. Imran Hossain, Ibrahim Khalil   +4 more
doaj   +2 more sources

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
doaj   +3 more sources

Progressive hemifacial atrophy: a case report. [PDF]

British Journal of Ophthalmology, 1985
A case of a 28-year-old Caucasian female with progressive hemifacial atrophy and atrophy of the rhomboid muscles on the ipsilateral side is reported. The literature on this condition and its treatment is reviewed.
exaly   +3 more sources