XX 남성 증후군 (Q365589)

Wikidata
둘러보기로 이동 검색으로 이동
rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases 영어
편집
언어 레이블 설명 다른 이름
한국어
XX 남성 증후군
설명이 없습니다.
    영어
    XX male syndrome
    rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases
    • De la Chapelle syndrome
    • 46,XX testicular disorders of sex development
    • 46,XX sex reversal
    • 46,XX DSD
    • nonsyndromic 46,XX testicular DSD
    • 46, XX gonadal sex reversal
    • 46,XX testicular difference of sex development
    • 46, XX testicular disorder of sex development
    • 46, XX testicular DSD
    • XX sex reversal

    서술

    식별자

    46, XX Testicular Disorders of Sex Development
    46, XX Gonadal Sex Reversal
    46, XX Testicular DSD
    46, XX Testicular Disorder of Sex Development
    Gonadal Sex Reversal, 46, XX
    Sex Reversal, Gonadal, 46, XX
    XX Male Syndrome
    XX Sex Reversal
    scope note 영어
    Congenital conditions in individuals in which male GONADS develop in a genetic female (female to male sex reversal). (영어)
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    De la Chapelle syndrome English
    XX male syndrome
    scope note 영어
    De la Chapelle syndrome causes people with XX chromosomes to be born with a penis and testes. This usually happens because a particular gene typically seen on Y chromosomes (known as the SRY gene) ends up on one of their X chromosomes and causes their genitals and internal reproductive organs to develop as they typically would in someone with XY chromosomes. People with de la Chapelle might have testes that are smaller than typical or that are undescended, and they are often infertile. In adolescence, they may experience breast growth, and they might not develop the characteristics that are usually associated with a typical testosterone puberty. (영어)
    0 개의 참고문헌
    0 개의 참고문헌
    LD52.0
    Male with 46,XX karyotype
    0 개의 참고문헌
    0 개의 참고문헌
    0 개의 참고문헌
    Orphanet ID 영어
    0 개의 참고문헌
     
    편집
      편집
        편집
          편집
            편집
              편집
                편집
                  편집