Arvelig leiomyomatose og nyrecellekreft (FH-relatert tumorpredisposisjon)
Autosomal dominant
FH-varianter som gir kutane og uterine leiomyomer og en risiko for papillær nyrecellekarsinom type 2.
Hva en diagnose endrer
Årlig MR av nyrene, vanligvis fra barne- eller ungdomsalderen, gir mulighet for tidlig oppdagelse og kirurgi; slektninger kan tilbys testing.
Analyserte gener
Også kjent 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
