Emerging Therapeutic Implications of STK11 Mutation: Case Series
نویسندگان
چکیده
منابع مشابه
Peutz-Jeghers syndrome with germline mutation of STK11
Peutz-Jeghers syndrome (PJS), also known as periorificial lentiginosis, is a rare autosomal dominant inherited disease with an incidence of 1/200,000 live-borns. Mutations in the serine-threonine kinase 11 (STK11) gene are considered the major cause of PJS. The most frequent complication at young age is recurrent intussusception due to multiple hamartomatous polyps, primarily in the small intes...
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ژورنال
عنوان ژورنال: The Oncologist
سال: 2020
ISSN: 1083-7159,1549-490X
DOI: 10.1634/theoncologist.2019-0846