Rare Diseases Symptoms Automatic Extraction

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

[cowden syndrome]

During the past few years, several genetic aberrations that may contribute to increased risks for development of breast and/or ovarian cancers have been identified. The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast and Ovarian focus specifically on the assessment of genetic mutations in BRCA1/BRCA2, TP53, and PTEN, and recommend approaches to genetic testing/counseling and management strategies in individuals with these mutations. This portion of the NCCN Guidelines includes recommendations regarding diagnostic criteria and management of patients with Cowden Syndrome/PTEN hamartoma tumor syndrome.

Diseases presenting "tumor syndrome" symptom

  • cowden syndrome
  • familial hypocalciuric hypercalcemia
  • lymphangioleiomyomatosis
  • pendred syndrome
  • proteus syndrome
  • von hippel-lindau disease
  • werner syndrome

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