Arvelig leiomyomatose og nyrecellekræft (FH-tumorprædisposition)
Autosomal dominant
FH-varianter, der forårsager kutane og uterine leiomyomer og en risiko for papillær nyrecellekarcinom type 2.
Hvad en diagnose ændrer
Årlig MR-scanning af nyrerne, typisk fra barndom eller ungdom, muliggør tidlig opdagelse og operation; slægtninge kan tilbydes test.
Analyserede gener
Også kendt som
familial leiomyomatosis; familial leiomyomatosis and renal cell cancer; familial leiomyomatosis cutis et uteri; familial leiomyomatosis with renal carcinoma; familial multiple cutaneous leiomyomas; hereditary leiomyomatosis; hereditary leiomyomatosis and renal cell cancer syndrome; Hereditary Leiomyomatosis and Renal Cell Carcinoma; hereditary leiomyomatosis with renal carcinoma; hereditary multiple cutaneous leiomyomas; HLRCC; leiomyomatosis and renal cell cancer; LRCC; MCUL; multiple cutaneous and uterine leiomyomas; multiple cutaneous and uterine leiomyomata; multiple cutaneous leiomyomata; Reed syndrome; Reed's syndrome
