멘델성 마이코박테리아 질환 감수성
IL12RB1, IL12B, IFNGR1, IFNGR2, STAT1, IRF8, ISG15 및 RORC 등의 유전자에 의해 발생하는 IL-12/인터페론-감마 경로의 유전적 결함입니다.
진단이 달라지는 점
해당 질환이 있는 분과 위험이 있는 가족은 BCG 및 기타 생백신 접종을 피하는 것이 좋습니다. 감염은 장기간의 치료가 필요하며, 일부 유형은 인터페론-감마 치료에 반응합니다.
다른 명칭
idiopathic infection caused by BCG or atypical mycobacteria; Mendelian susceptibility to atypical mycobacteria; Mendelian susceptibility to mycobacterial infections; MSMD; Mycobacterium caused genetic susceptibility to infections due to particular pathogens; Mycobacterium genetic susceptibility to infections due to particular pathogens
관련 하위 유형 15개 포함 ↓하위 유형 숨기기 ↑
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
- autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
- immunodeficiency 27A
- Mendelian susceptibility to mycobacterial diseases due to a complete deficiency
- Mendelian susceptibility to mycobacterial diseases due to a partial deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
- Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
- Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
- X-linked Mendelian susceptibility to mycobacterial diseases
- X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
