Clinical Guidelines for Diagnosis and Management of Juvenile Polyposis Syndrome in Children and Adults―Secondary Publication

Juvenile polyposis syndrome (JPS) is a rare disease characterized by multiple hamartomatous polyps within the gastrointestinal tract. SMAD4 or BMPR1A is known as a causative gene of JPS. Approximately 75% of newly diagnosed cases have an autosomal-dominantly inherited condition, whereas 25% are spor...

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Detalles Bibliográficos
Autores principales: Matsumoto, Takayuki, Umeno, Junji, Jimbo, Keisuke, Arai, Masami, Iwama, Itaru, Kashida, Hiroshi, Kudo, Takahiro, Koizumi, Koichi, Sato, Yasushi, Sekine, Shigeki, Tanaka, Shinji, Tanakaya, Kohji, Tamura, Kazuo, Hirata, Keiji, Fukahori, Suguru, Esaki, Motohiro, Ishikawa, Hideki, Iwama, Takeo, Okazaki, Yasushi, Saito, Yutaka, Matsuura, Nariaki, Mutoh, Michihiro, Tomita, Naohiro, Akiyama, Takashi, Yamamoto, Toshiki, Ishida, Hideyuki, Nakayama, Yoshiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Society of Coloproctology 2023
Materias:
Practice Guideline
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129355/
https://www.ncbi.nlm.nih.gov/pubmed/37113581
http://dx.doi.org/10.23922/jarc.2023-002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129355/
https://www.ncbi.nlm.nih.gov/pubmed/37113581
http://dx.doi.org/10.23922/jarc.2023-002

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