Hereditary Leiomyomatosis Renal Cell Cancer (HLRCC): Identification of the Disease Gene, and Characterization of the Predisposition to Renal Cancer
Condition: Renal Tumor Histology, Cutaneous Leiomyoma, Kidney Cancer
Study Type: Observational
Clinical Trials Identifier NCT 8-digits: NCT00050752
Sponsor: National Cancer Institute (NCI)
Phase:
Eligibility:
- Age: minimum 2 Years maximum N/A
- Gender: All
Inclusion Criteria:
- Individuals suspected or known to have phenotype or genotype suggestive of Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome (HLRCC), such as:
- Cutaneous leiomyoma and kidney cancer; or
- Cutaneous leiomyoma and uterine leiomyoma; or
- Multiple cutaneous leiomyoma; or
- Kidney cancer and uterine leiomyomata; or
- Renal tumor histology consistent with HLRCC including, but not limited to: Collecting Duct and/or Papillary, Type II
- All participants and parents/guardians, for children younger than 18 years of age, must sign an informed consent document indicating their understanding of the investigational nature and the risks of this study before any protocol related studies are performed.
- Participants must be >= 2 years of age.
- A relative (related by blood) of an individual with a confirmed or suspected diagnosis of HLRCC.
Exclusion Criteria:
- None
View trial on ClinicalTrials.gov