Results 61 to 70 of about 1,924 (163)
S2k guideline: Diagnosis and therapy of localized scleroderma
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter +12 more
wiley +1 more source
Forehead reconstruction with a custom-made three-dimensional titanium implant in a Parry-Romberg syndrome patient [PDF]
, 2018 Parry-Romberg syndrome is a rare neurocutaneous syndrome characterized by progressive shrinkage and degeneration of the tissues usually on only one side of the face. It is usually difficult to restore the facial contour due to skin tightness.
정복기 +4 more
core +1 more source
Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report
Arquivos de Neuro-Psiquiatria, 1995 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
S2k‐Leitlinie: Diagnostik und Therapie der zirkumskripten Sklerodermie
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-621, April 2024.Zusammenfassung Die vorliegende aktualisierte S2k‐Leitlinie befasst sich mit der Diagnostik und der Therapie der zirkumskripten Sklerodermie (ZS). Diese umfasst ein Spektrum sklerotischer Erkrankungen der Haut mit, je nach Subtyp und Lokalisation, möglicher Beteiligung von hautnahen Strukturen wie Fettgewebe, Muskulatur, Gelenke und Knochen. Ein Befall
Alexander Kreuter +12 more
wiley +1 more source
Facial hemiatrophy: Review of literature and a case report
Journal of Indian Academy of Oral Medicine and Radiology, 2011 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
Systematic Review of Health‐Related Quality of Life Impact in Juvenile Localized Scleroderma
Arthritis Care &Research, Volume 76, Issue 3, Page 340-349, March 2024.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
, 2006 Parry–Romberg syndrome is a rare disorder of unknown aetiology that involves slowly progressive but self-limited wasting of subcutaneous tissues on one side of the face, usually in the distribution of a branch of the trigeminal nerve.
Drummond, P.D., Finch, P.M., Hassard, S.
core
Anesthetic Considerations of Patient with Parry Romberg Syndrome
Case Reports in Clinical Practice, 2018 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
International Wound Journal, Volume 21, Issue 1, January 2024.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
Parry-Romberg syndrome: A case report of non-invasive treatment
, 2019 Parry-Romberg syndrome is an uncommon condition, self-limiting with slow progressive hemifacial atrophy. This syndrome can lead to several progressive congenital and developmental deformities. It can cause severe facial asymmetry and subsequently lead to
Zahra Tehrani +4 more
core +1 more source