Results 61 to 70 of about 1,281,448 (141)
Progressive Hemifacial Atrophy (Parry-Romberg Syndrome)
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 +1 more source
Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report
Os autores apresentam o caso de uma paciente de 45 anos de idade com história de 15 meses de evolução, de hemiatrofia progressiva da face e língua à esquerda.
Nicandro De Figueiredo Neto +3 more
doaj +1 more source
Systematic Review of Health‐Related Quality of Life Impact in Juvenile Localized Scleroderma
Objective The prevalence and types of psychosocial complications of juvenile localized scleroderma (JLS), also known as morphea, an inflammatory and sclerosing disease involving the skin, fascia, muscle, and bone, are poorly understood. Methods We performed a systematic review of literature published between 2000 and 2020 in PubMed, EMBASE, the ...
Luis F. Sanchez‐Espino +5 more
wiley +1 more source
Parry Romberg Syndrome: a case report
Parry Romberg syndrome (PRS) is a rare disorder, characterized by unilateral facial atrophy of the skin, subcutaneous fat, muscles, cartilages, and even bone. Various systemic manifestations reported with this syndrome are neurologic, maxillofacial, and ophthalmologic. The etiology is still unknown.
Ahmad Liaquat +2 more
openaire +1 more source
Anesthetic Considerations of Patient with Parry Romberg Syndrome
Parry Romberg syndrome is a rare progressive degenerative disease characterized by unilateral atrophy affecting the skin, connective tissue, muscle, and bone, typically occurs in children and young adults.
Sussan Soltani Mohammadi +2 more
doaj
Abstract Localised scleroderma predominantly affects the skin with an unknown aetiology. Despite its clinical importance, no comprehensive bibliometric analysis has been conducted to assess the existing research landscape and future prospects for localised scleroderma. The articles related to localised scleroderma were retrieved from the WoSCC database
Zi‐Ming Li +5 more
wiley +1 more source
Facial hemiatrophy: Review of literature and a case report
A case report of hemifacial atrophy is presented in this paper. It is also known as Parry-Romberg syndrome, is an uncommon degenerative and poorly understood condition.
Manisha S Tijare +4 more
doaj +1 more source
Parry-Romberg Syndrome with Intracranial Vascular Dysplasia: A case report [PDF]
Parry-Romberg syndrome is characterized by slowly progressive but self-limited atrophy of the facial subcutaneous fat, which can be followed by wasting of associated skin, cartilage, connective or ocular tissue, muscle and bone.
신지철, 박창일
core
Waardenburg syndrome: A rare case
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, it compromises approximately 2-5% of congenital deaf children.
Shivlal M Rawlani +3 more
doaj +1 more source
Parry-Romberg Syndrome: Presentation of Two Patients; Review of Neuro-Ophthalmologic Manifestations
Reports the neuro-ophthalmologic associations in patients with Parry-Romberg syndrome are ...
Warren Felton; Scott Haines
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