Morphea
☆ In die 2022 Stiftung Warentest-resultate van Duitsland was verbruikerstevredenheid met ModelDerm net effens laer as met betaalde telemedisyne-konsultasies.
Die letsel van Morphea verskyn gewoonlik as 'n atrofiese gepigmenteerde kol.
References
Scleroderma is 'n seldsame siekte wat bindweefsel aantas, wat as verharde vel verskyn en soms ander dele van die liggaam beïnvloed. Daar is twee hooftipes: systemic sclerosis , wat velverharding en interne organe behels, en localized scleroderma , ook bekend as morphea, wat tipies beperk bly tot die vel en weefsels daaronder, met 'n goedaardige en selfbeperkende verloop. Alhoewel gelokaliseerde skleroderma ongewoon is en die oorsaak daarvan onduidelik is, dui onlangse navorsing daarop dat dit ook interne organe kan beïnvloed en tot verskeie gesondheidskwessies kan lei. Vroeë behandeling is noodsaaklik om komplikasies te voorkom, gegewe die potensiële erns van localized scleroderma.
Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma.
Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma.
Morphea , ook bekend as gelokaliseerde skleroderma, is 'n seldsame outo-immuun siekte wat bindweefsel aantas. Dit kan op verskillende maniere verskyn, en dit is nie baie algemeen nie, met ongeveer 0. 4 - 2. 7 gevalle per 100 000 mense elke jaar. Morphea word dikwels gesien by kinders tussen 2 en 14 jaar oud, en dit is geneig om meisies meer dikwels as seuns te beïnvloed.
Morphea (localized scleroderma) is a rare autoimmune connective tissue disease with variable clinical presentations, with an annual incidence of 0.4-2.7 cases per 100,000. Morphea occurs most frequently in children aged 2-14 years, and the disease exhibits a female predominance.
Morphea (localized scleroderma) is a rare autoimmune connective tissue disease with variable clinical presentations, with an annual incidence of 0.4-2.7 cases per 100,000. Morphea occurs most frequently in children aged 2-14 years, and the disease exhibits a female predominance.
Morphea is 'n baie seldsame siekte. As gevolg van die samestelling van die foto, het die algoritme dit dalk met morphea verwar.