Literature DB >> 24051481

Lynch syndrome: a pediatric perspective.

Sherry C Huang1, Carol A Durno, Steven H Erdman.   

Abstract

Colorectal cancer is a rare disease in the pediatric age group and, when present, suggests an underlying genetic predisposition. The most common hereditary colon cancer susceptibility condition, Lynch syndrome (LS), previously known as hereditary nonpolyposis colorectal cancer, is an autosomal dominant condition caused by a germline mutation in 1 of 4 DNA mismatch repair (MMR) genes: MLH1, MSH2, MSH6, or PMS2. The mutation-prone phenotype of this disorder is associated with gastrointestinal, endometrial, and other cancers and is now being identified in both symptomatic adolescents with malignancy as well in asymptomatic mutation carriers who are at risk for a spectrum of gastrointestinal and other cancers later in life. We review the DNA MMR system, our present understanding of LS in the pediatric population, and discuss the newly identified biallelic form of the disease known as constitutional mismatch repair deficiency syndrome. Both family history and tumor characteristics can help to identify patients who should undergo genetic testing for these cancer predisposition syndromes. Patients who carry either single allele (LS) or double allele (constitutional mismatch repair deficiency syndrome) mutations in the MMR genes benefit from cancer surveillance programs that target both the digestive and extraintestinal cancer risk of these diseases. Because spontaneous mutation in any one of the MMR genes is extremely rare, genetic counseling and testing are suggested for all at-risk family members.

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Year:  2014        PMID: 24051481     DOI: 10.1097/MPG.0000000000000179

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  4 in total

Review 1.  Syndrome-Associated Tumors by Organ System.

Authors:  Raul S Gonzalez; Nicole D Riddle
Journal:  J Pediatr Genet       Date:  2016-03-09

2.  Biallelic Mismatch Repair Deficiency in an Adolescent Female.

Authors:  Amber Hildreth; Mark A Valasek; Irene Thung; Thomas Savides; Mamata Sivagnanam; Sonia Ramamoorthy; Sherry C Huang
Journal:  Case Rep Genet       Date:  2018-07-25

3.  High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53.

Authors:  Vania Balderrama Brondani; Luciana Montenegro; Amanda Meneses Ferreira Lacombe; Breno Marchiori Magalhães; Mirian Yumie Nishi; Mariana Ferreira de Assis Funari; Amanda de Moraes Narcizo; Lais Cavalca Cardoso; Sheila Aparecida Coelho Siqueira; Maria Claudia Nogueira Zerbini; Francisco Tibor Denes; Ana Claudia Latronico; Berenice Bilharinho Mendonca; Madson Queiroz Almeida; Antonio Marcondes Lerario; Ibere Cauduro Soares; Maria Candida Barisson Villares Fragoso
Journal:  Cancers (Basel)       Date:  2020-03-07       Impact factor: 6.639

4.  Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors-A Cohort Study.

Authors:  Kshama Aswath; James Welch; Sriram Gubbi; Padmasree Veeraraghavan; Shirisha Avadhanula; Sudheer Kumar Gara; Esra Dikoglu; Maria Merino; Mark Raffeld; Liqiang Xi; Electron Kebebew; Joanna Klubo-Gwiezdzinska
Journal:  Front Endocrinol (Lausanne)       Date:  2021-07-13       Impact factor: 5.555

  4 in total

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