MLH1 c.199G>A, a Known Mutation for Lynch Syndrome, Is Also Associated with Sebaceous Neoplasm
Abstract. Introduction:. Muir-Torre syndrome is a phenotypic variant of Lynch syndrome characterized by a predisposition for the development of visceral malignant disease and sebaceous gland neoplasms, and it is caused by germline mutations in the mismatch repair genes MSH2 and MLH1. Here, we report...
Main Authors: | Wei-Sheng Li, Yan Li, Nai-Hui Zhou, Jing-Liu Liu, Zi-Liang Yang, Miao Sun, Min Li |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Health
2021-06-01
|
Series: | International Journal of Dermatology and Venerology |
Online Access: | http://journals.lww.com/10.1097/JD9.0000000000000139 |
Similar Items
-
Sebaceous neoplasms in Lynch syndrome
by: Dandapani Monica, et al.
Published: (2011-03-01) -
A Chinese family affected by lynch syndrome caused by MLH1 mutation
by: Shuqin Jia, et al.
Published: (2018-06-01) -
Common mutations identified in the MLH1 gene in familial Lynch syndrome
by: Jisha Elias, et al.
Published: (2017-12-01) -
Novel Mutations in MLH1 and MSH2 Genes in Mexican Patients with Lynch Syndrome
by: Jose Miguel Moreno-Ortiz, et al.
Published: (2016-01-01) -
Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome
by: Peter Georgeson, et al.
Published: (2019-07-01)