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FAMMM syndrome

Familial Atypical Multiple Mole Melanoma Syndrome Dysplastic nevus syndromeFamilial melanomaB-K mole syndrome
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "FAMMM syndrome" returned 0 free, full-text review articles. First 0 results:
Pancreatic cancer and the FAMMM syndrome.
Last Updated: Nov 13, 2018

Hereditary cancer syndromes provide excellent models for molecular genetic studies that may aid significantly in case detection, surveillance, and management. Ultimately, molecularly based designer pharmaceuticals may emerge from this research, such as the case of trastuzumab (Herceptin) ...

FAMMM syndrome: pathogenesis and management.
Last Updated: Sep 06, 2019

Familial atypical multiple mole melanoma (FAMMM) syndrome is an autosomal dominant disorder with variable incomplete penetrance of the clinical phenotypes. Pathogenesis of this syndrome has not been fully investigated. Across multiple studies, germline mutations in the INK4a antioncogene ...

The FAMMM syndrome: epidemiology and surveillance strategies.
Last Updated: Sep 15, 2019

Research into the epidemiology of the melanoma-prone FAMMM syndrome, molecular genetics of the occurrences of melanoma, the photobiology of DNA damage/repair, diagnostic epiluminescence, microscopic/imaging techniques, and a new concept of photoprotection have altered melanoma strategies ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "FAMMM syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "FAMMM syndrome" returned 8 free, full-text research articles. First few results:
Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneity.
Last Updated: Dec 10, 2019

Approximately 5-10 % of cutaneous melanoma occurs in kindreds with a hereditary predisposition. Mutations in the CDKN2A gene are found to occur in approximately 20-40 % of these kindreds. The first historical mention of what is now called the familial atypical multiple mole melanoma ...

Multiple primary cutaneous melanomas in patients with FAMMM syndrome and sporadic atypical mole syndrome (AMS): what's worse?
Last Updated: Nov 13, 2018

Atypical Mole Syndrome is the most important phenotypic risk factor for cutaneous melanoma, a malignancy that accounts for about 80% of deaths from skin cancer. Since early diagnosis of melanoma is of great prognostic relevance, the identification of Atypical Mole Syndrome carriers ...

Multiple neurofibromas as the presenting feature of familial atypical multiple malignant melanoma (FAMMM) syndrome.
Last Updated: May 24, 2013

Mutations in the cyclin-dependent kinase inhibitor-2A (CDKN2A) gene have been associated with a number of malignancies, most notably cutaneous malignant melanoma (CMM). Mutations in this gene have also been associated with pancreatic cancer and breast cancer, as well as astrocytomas ...

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