Abstract

Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. Conversely, recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be important for the same reason. The Familial Cancer Database (FaCD) is a web-based application which has been developed at our department with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients. This encyclopaedia is published in parts and discusses the disorders included in the FaCD database in alphabetical order. It lists names, synonyms, OMIM number, mode of inheritance, associated genes, phenotype, clinical discussion and references. The purpose of presenting this encyclopaedia in paper format is simply that we hope that you as clinicians and researchers find it helpful to browse through it and familiarize yourself even better with the scope of genetic disorders that have been associated with increased tumour risk.

Highlights

  • Cancer is associated with a wide range of hereditary disorders

  • Recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be important for the same reason

  • The Familial Cancer Database (FaCD) is a web-based application which has been developed at the Department of Genetics of the University Medical Center Groningen, The Netherlands, with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients

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Summary

Introduction

Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. The Familial Cancer Database (FaCD) is a web-based application (www.facd.info) which has been developed at the Department of Genetics of the University Medical Center Groningen, The Netherlands, with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients. This encyclopaedia is published in parts and discusses the disorders included in the FaCD database in alphabetical order. Somatic GNAS1 mutations have been observed in isolated AIMAH cases

Adenosine deaminase deficiency
Aicardi syndrome
Alagille syndrome
Alport syndrome with diffuse leiomyomatosis
Androgen insensitivity syndrome
Ataxia pancytopenia syndrome
Ataxia telangiectasia
Basal cell nevus syndrome
Bazex syndrome
Biallelic mismatch repair gene mutations associated early onset cancer
Bloom syndrome
Blue rubber bleb nevus syndrome
Byler disease
Cardiofaciocutaneous syndrome
Carney complex
Carney triad
Caroli disease
Cerumen type
Cheilitis glandularis
Findings
CHIME syndrome

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