Morphea
☆ AI Dermatology — Free Service
Natiijooyinka Stiftung Warentest ee 2022 ee ka yimid Jarmalka, ku qanacsanaanta macaamilka ee ModelDerm ayaa waxyar uun ka hooseysay la-talinta telemedicine-ka ee lacagta lagu bixiyo.
Natiijooyinka Stiftung Warentest ee 2022 ee ka yimid Jarmalka, ku qanacsanaanta macaamilka ee ModelDerm ayaa waxyar uun ka hooseysay la-talinta telemedicine-ka ee lacagta lagu bixiyo.
Nabarka Morphea badanaa wuxuu u muuqdaa balastar midab leh.
relevance score : -100.0%
ReferencesScleroderma waa cudur naadir ah oo saameeya unugyada isku xira, wuxuuna u muuqdaa sidii maqaar adag oo mararka qaar saameeya qaybaha kale ee jirka. Waxaa jira laba nooc oo waaweyn: systemic sclerosis, oo ku lug leh qallafsanaanta maqaarka iyo xubnaha gudaha, iyo localized scleroderma, oo sidoo kale loo yaqaan morphea, taas oo caadi ahaan ku xaddidan maqaarka iyo unugyada hoostiisa, iyadoo leh kooras aan fiicnayn oo si iskiis ah u xaddidan. Inkasta oo cudurka 'scleroderma' ee maxalliga ah uu yahay mid aan caadi ahayn oo aan la garanayn sababta keentay, cilmi-baaris dhawaan ah ayaa soo jeedinaysa inay sidoo kale saameyn karto xubnaha gudaha oo ay keento arrimo caafimaad oo kala duwan. Daawaynta hore waa muhiim si looga hortago dhibaatooyinka, iyadoo la tixgelinayo halista suurtagalka ah ee 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, oo sidoo kale loo yaqaan 'scleroderma localized', waa cudur naadir ah oo nidaamka difaaca jirka ah oo saameeya unugyada isku xiran. Waxay u soo bixi kartaa siyaabo kala duwan, mana aha wax caadi ah; qiyaastii 0.4 – 2.7 kiis per 100,000 qof sanadkii. Morphea inta badan waxaa lagu arkaa carruurta da'doodu u dhaxaysa 2 ilaa 14 sano, waxayna u badan tahay inay saameyn ku yeelato gabdhaha ka badan wiilasha.
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 waa cudur aad u dhif ah. Sababo la xiriira muuqaalka sawirka, algorithm‑ka waxa laga yaabaa inuu si qalad ah u aqoonsado morphea.