Morphea
☆ A cikin sakamakon Stiftung Warentest na 2022 daga Jamus, gamsuwar mabukaci tare da ModelDerm ya ɗan yi ƙasa kaɗan fiye da biyan shawarwarin telemedicine.
Ciwon Morphea yawanci yana bayyana azaman faci mai launi.
References
Scleroderma cuta ce da ba kasafai take shafar sassan jiki ba, tana nunawa kamar taurin fata kuma wani lokacin tana shafar wasu sassan jiki. Akwai manyan nau'ikan guda biyu: systemic sclerosis , wanda ya ƙunshi taurin fata da gabobin ciki, da kuma localized scleroderma , wanda kuma aka sani da morphea, wanda yawanci yakan tsaya ga fata da kyallen da ke ƙarƙashinta, tare da tsari mara kyau kuma mai karewa. Kodayake scleroderma na gida ba sabon abu ba ne kuma ba a san dalilinsa ba, bincike na baya-bayan nan ya nuna yana iya shafar gabobin ciki kuma ya haifar da lamuran lafiya daban-daban. Magani da wuri yana da mahimmanci don hana rikitarwa, idan aka yi la'akari da yiwuwar 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 , wanda kuma aka sani da scleroderma na gida, cuta ce mai saurin kamuwa da cuta wacce ke shafar nama. Yana iya bayyana ta hanyoyi daban-daban, kuma ba a saba da shi ba, tare da kusan 0. 4 - 2. 7 a kowane mutum 100,000 kowace shekara. Ana yawan ganin Morphea a cikin yara tsakanin shekaru 2 zuwa 14, kuma yana shafar yara mata fiye da maza.
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 cuta ce da ba kasafai ba. Saboda abun da ke cikin hoton, algorithm na iya kuskuren shi don morphea.