基因检测
遗传咨询
植入前遗传学诊断
社会心理的
疾病
医学
预测性试验
无症状的
遗传条件
心理学
怀孕
精神科
遗传学
儿科
生物
病理
作者
Rachel Paul,Aaron Baldwin,K. E. Johnson,Sara Manning Peskin,Thomas F. Tropea,Meron Azage,Tanya Bardakjian,Laynie Dratch
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2023-11-07
卷期号:101 (19): 836-841
标识
DOI:10.1212/wnl.0000000000207736
摘要
Preimplantation genetic testing for monogenic conditions (PGT-M), formerly called preimplantation genetic diagnosis, is a specialized assisted reproduction technique that aims to reduce the risk of a pregnancy inheriting a monogenic condition. Despite calls to increase awareness and prepare neurologists for discussing PGT-M with patients and their families, no guidelines currently exist. When introducing PGT-M to those who may be interested in using it, there are major factors for discussion, including (1) genetic considerations (e.g., requirement for a confirmed genetic diagnosis; timing of genetic test results); (2) practical considerations (e.g., access to PGT-M and genetic services); (3) technical considerations (e.g., factors that can affect the success rate of PGT-M); and (4) psychosocial and ethical considerations (e.g., predictive testing for asymptomatic family members; family dynamics and values). Here, our team of neurologists and specialized genetic counselors discusses the current state of genetic characterization in adult-onset neurodegenerative conditions and highlights the major factors that should be considered when discussing PGT-M with families.
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