Morphea
☆ Yn 'e 2022 Stiftung Warentest-resultaten út Dútslân wie de konsuminttefredenheid mei ModelDerm mar wat leger dan mei betelle telemedisynkonsultaasjes.
De lesion fan Morphea ferskynt meastentiids as in atrofysk pigmente plak.
References
Scleroderma is in seldsume sykte dy't bindeweefsels beynfloedet, ferskynt as ferhurde hûd en soms beynfloedet oare dielen fan it lichem. D'r binne twa haadtypen: systemic sclerosis , wêrby't hûdferharding en ynterne organen omfettet, en localized scleroderma , ek bekend as morphea, dy't gewoanlik beheind bliuwt ta de hûd en weefsels derûnder, mei in goedaardige en selsbeheinende kursus. Hoewol lokalisearre skleroderma ûngewoan is en de oarsaak ûndúdlik is, suggerearret resint ûndersyk dat it ek ynterne organen kin beynfloedzje en liede ta ferskate sûnensproblemen. Iere behanneling is krúsjaal om komplikaasjes te foarkommen, sjoen de potinsjele earnst fan 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 , ek wol lokalisearre skleroderma neamd, is in seldsume autoimmune sykte dy't bindeweefsel beynfloedet. It kin op ferskate manieren ferskine, en it is net heul gewoan, mei sawat 0. 4 - 2. 7 gefallen per 100. 000 minsken elk jier. Morphea wurdt faak sjoen by bern tusken 2 en 14 jier âld, en it hat de neiging om famkes faker te beynfloedzjen dan jonges.
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 in tige seldsume sykte. Troch de gearstalling fan 'e foto kin it algoritme it fersin hawwe mei morphea.