医学
林奇综合征
DNA错配修复
神经纤维瘤病
基因检测
疾病
遗传学
突变
儿科
基因
生物
病理
内科学
DNA修复
作者
Kelly Winter,Martin Tan,Eric Briscoe,A Hyde,Stanley John
出处
期刊:American Surgeon
[SAGE Publishing]
日期:2023-06-01
卷期号:89 (9): 3953-3955
被引量:1
标识
DOI:10.1177/00031348231173987
摘要
Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caused by biallelic heterozygous defects: distinct deleterious mutations on each allele for a single gene. As the disease is exceedingly rare and may present via a wide variety of signs, including neurofibromatosis type 1- and Lynch Syndrome-associated malignancies, diagnosis and subsequent surveillance are complex with suggested methods published by the International Replication Repair Deficiency Consortium. We report here the history and management of a patient whose newly diagnosed CMMRD was managed with both curative and prophylactic surgical treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI