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CS

Gorlin Syndrome

Czech version

Authors: P. Plevová ¹; V. Krutílková ²; A. Puchmajerová ³; L. Foretová ⁴
Authors‘ workplace: Ústav patologie & Laboratoř molekulární patologie LF UP Olomouc 2Gennet s. r. o., Praha 3Ústav biologie a lékařské genetiky FN Motol Praha 4Masarykův onkologický ústav Brno ; Oddělení lékařské genetiky FN Ostrava ¹
Published in: Klin Onkol 2009; 22(Supplementum): 34-35

Sources

1. Lindor NM, Greene MH a Mayo Familial Cancer Program. The concise handbook of family cancer syndromes. J Natl Cancer Inst 1998; 90: 1039–1071.

2. Doporučení dle American College of Medical Genetists.

3. www.en.wikipedia.org

4. www.emedicine.com

Labels

Paediatric clinical oncology Surgery Clinical oncology

Hereditary Breast and Ovarian Cancer Syndrome

Hereditary Nonpolyposis Colorectal Cancer (HNPCC, Lynch syndrome)

Familial Adenomatous Polyposis

Li-Fraumeni Syndrome

Von Hippel-Lindau Disease

Multiple Endocrine Neoplasia Type 1 Syndrome

Multiple Endocrine Neoplasia Type 2 Syndrome

Familial Atypical Multiple Mole Melanoma Syndrome – FAMMM

Peutz-Jeghers Syndrome

The Survey of Syndromes with the Risk of Cancer in Children Age

Tuberous Sclerosis

Hereditary Pancreatitis

Cowden Syndrome

Recommendation for Prophylactic Surgery for Decreasing the Risk of Gynaecological Cancer in Women with Hereditary Risk

Current Methods in Diagnostics and Monitoring of Patients with Hereditary Polyposis Syndromes. Investigation of the Small Intestine

Limitations of Genetic Testing in Oncology

Prerequisites for Preimplantation Genetic Diagnosis (PGD) in Carriers of Mutations Responsible for Hereditary Cancers

Commentary: Preimplantation Genetic Diagnosis

Commentary: The Possibilities of (Assisted Reproduction Techniques) in Control of Risk Genes Transfer to the Offspring

Commentary: Preimplantation Genetic Diagnosis

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