Hereditary leiomyomatosis and renal cell cancer (FH tumour predisposition)
Autozomálně dominantní
FH variants causing cutaneous and uterine leiomyomas and a risk of type 2 papillary renal cell carcinoma.
Co se diagnózou změní
Annual kidney MRI, usually from childhood or adolescence, allows early detection and surgery; relatives can be offered testing.
Analyzované geny
Známé také jako
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
