Results 71 to 80 of about 28,795 (192)
Delayed diagnosis of adult indolent systemic mastocytosis
Systemic mastocytosis (SM) is a rare, heterogeneous disorder characterized by infiltration and accumulation of mast cells within multiple organs, most commonly the skin. Given the rarity of the disease and the fact that many of its symptoms are shared by
Carsten Sauer Mikkelsen +3 more
doaj +1 more source
El mastocito y la mastocitosis
Se efectúa una revisión de la morfología, bioquímica y funciones del mastocito, célula completa que juega un rol central en las reacciones de hipersensibilidad, pero también en otros cuadros patológicos (urticaria, diátesis atópica, hemangiomas ...
Carlos Escobar R
doaj
We present a case of a 2-year-old girl with urticaria pigmentosa. The clinical features indicated disseminated, discrete, non-clustered, reddish-brown macules, papules, and plaques on her body (0.5-1 cm in diameter).
Ahmed Hassan Al-Ghamdi +4 more
core +1 more source
Mast cell disorders are defined by an abnormal accumulation of tissue mast cells in one or more organ systems. In systemic mastocytosis, at least one extracutaneous organ is involved by definition.
Didem Ozdemir +6 more
doaj +1 more source
Mastocitosis. Presentación de un caso
La mastocitosis o mastocitoma es una genodermatosis poco frecuente, de etiología desconocida, incluida en el grupo de "enfermedades raras", que aparece en la infancia generalmente.
Carlos Alberto Blanco Córdova
doaj
Um Novo Olhar sobre a Telangiectasia Macularis Eruptiva Perstans
A telangiectasia macularis eruptiva perstans (TMEP) é uma forma rara de mastocitose cutânea com semiologia e histologia próprias, mas não isenta de controvérsia em relação à sua individualização enquanto entidade nosológica.
André Pinho +4 more
doaj +1 more source
Adult urticaria pigmentosa: successful treatment in association with phototherapy
Introdução: A urticária pigmentosa em adultos é uma forma de mastocitose rara e persistente, frequentemente com manifestações sistêmicas e acometimento da medula óssea, e manifestações cutâneas menos evidentes, ao contrário do que ocorre na infância ...
Morgado de Abreu, Marilda Aparecida Milanez +2 more
core +1 more source
Mutation-independent treatment of autosomal dominant Retinitis Pigmentosa (adRP) [PDF]
Viral-mediated gene therapy holds great promise for the treatment of severe inherited retinal diseases, such as Retintitis Pigmentosa (RP), which is caused by mutations in genes preferentially expressed in photoreceptor cells. The availability of vectors
Mussolino, Claudio
core +1 more source

