Cargando…
"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear scleroderma "en coup de sabre" with CNS tumor
BACKGROUND: Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with limited scleroderma linearis. Linear scleroderma "en coup de sabre" is characterized by clinical presence of most commonl...
Autores principales: | Bergler-Czop, Beata, Lis-Święty, Anna, Brzezińska-Wcisło, Ligia |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723072/ https://www.ncbi.nlm.nih.gov/pubmed/19635150 http://dx.doi.org/10.1186/1471-2377-9-39 |
Ejemplares similares
-
Parry-Romberg Syndrome with En Coup de Sabre
por: Jun, Jae Hun, et al.
Publicado: (2011) -
Parry-Romberg Syndrome Associated with Localized Scleroderma
por: Maletic, Jelena, et al.
Publicado: (2010) -
P08 Appearance matters: a case of adult-onset Parry-Romberg syndrome with linear scleroderma en coup de sabre and neurological involvement
por: Syrimi, Zoe, et al.
Publicado: (2023) -
Antiphospholipid antibodies in localized scleroderma: the potential role of screening tests for the detection of antiphospholipid syndrome
por: Lis-Święty, Anna, et al.
Publicado: (2014) -
3D stereophotogrammetry in children and adolescents with Scleroderma En Coup De Sabre/Parry‐Romberg Syndrome: Description of a novel method for monitoring disease progression
por: ter Horst, Rutger, et al.
Publicado: (2022)