Hereditary Neoplastic Syndromes

Adenomatous polyposis coli is a protein encoded by the APC gene and acts as a tumor suppressor. Discover the latest research on adenomatous polyposis coli here.

Multiple Hamartoma Syndrome, also known as Cowden disease, is a hereditary autosomal dominant condition associated with mutations in tumor suppressor PTEN. Here is the latest research.

Hereditary breast and ovarian cancer due to mutations in the brca1 and brca2 genes is the most common cause of hereditary forms of both breast and ovarian cancer. Here are the latest discoveries pertaining to these cancers.

Hereditary cancer syndromes comprise 5% of all cancers and have an increased risk of early onset and of multiple or bilateral malignancies. Here is the latest research on hereditary cancer syndromes.

Hereditary Nonpolyposis Colorectal Neoplasms are a type of inherited autosomal dominant colon cancer and is associated with mutations in mismatch repair genes. Discover the latest research on Hereditary Nonpolyposis Colorectal Neoplasms.

Li-Fraumeni syndrome in an inherited predisposition to a range of cancers due to a mutation in the tumor suppressor gene TP53. The diagnosis is made if cancer occurs at a young age and there is also a family history of sarcoma or cancer at a young age. Find the latest research on Li-Fraumeni syndrome here.

Multiple Endocrine Neoplasia is a group of inherited autosomal dominant cancers that occur in multiple hormone producing grandular organs. Discover the latest research on Multiple Endocrine Neoplasia here.

Neurofibromatosis is a genetic disorder that causes tumors to form in the central nervous system. While these tumors are typically benign, they can become malignant. Other complications of neurofibromatosis include hearing loss, learning impairment, vision loss, etc. Here is the latest research.

Neurofibromatosis 1 (NF1), also known as von Recklinghausen disease, is an autosomal dominant condition caused by mutations in the NF1 gene. Here is the latest research.

Type 2 Neurofibromatosis are rare inherited autosomal dominant diseases caused by the NF2 gene. It is characterized by the growth of noncancerous tumors in the nervous system, specifically along the auditory nerve. Symptoms include hearing loss, tinnitus, and balance problems. Here is the latest research on Type 2 Neurofibromatosis.

Peutz–Jeghers syndrome (PJS) is an autosomal dominant genetic disorder characterized by benign gastrointestinal polyps and melanosis. Discover the latest research on PJS here.

Tuberous Sclerosis (TSC) is an autosomal dominant genetic disorder caused by mutations in TSC1 or TSC2 tumor suppressor genes and characterized by the development of benign hamartomas in multiple organs. Here is the latest research.

Wilms’ tumor, also known as nephroblastoma, is a specific type of cancer that begins in the kidneys and primarily in children. This is the most common type of kidney cancer found in children. Treatment options provide good prognosis for this disease. Discover the latest research on Wilms’ tumor here.