Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.
Juvenile polyposis syndrome (JPS) is an inherited hamartomatous-polyposis syndrome with a risk for colon cancer. JPS is a clinical diagnosis by exclusion, and, before susceptibility genes were identified, JPS could easily be confused with other inherited hamartoma syndromes, such as Bannayan-Riley-R...
Main Authors: | Zhou, X, Woodford-Richens, K, Lehtonen, R, Kurose, K, Aldred, M, Hampel, H, Launonen, V, Virta, S, Pilarski, R, Salovaara, R, Bodmer, W, Conrad, B, Dunlop, M, Hodgson, S, Iwama, T, Järvinen, H, Kellokumpu, I, Kim, J, Leggett, B, Markie, D, Mecklin, J, Neale, K, Phillips, R, Piris, J, Rozen, P |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2001
|
Similar Items
-
Germline mutations in BMPR1A/ALK3 cause a subset of cases of Juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
by: Zhou, X, et al.
Published: (2001) -
A rare case of Bannayan-Riley-Ruvalcaba syndrome with concurrent arteriovenous malformation
by: Rina Li, BA, et al.
Published: (2024-04-01) -
Bannayan-Riley-Ruvalcaba Syndrome in a Case Evaluated Due to Multinodular Goiter
by: Özlem Korkmaz, et al.
Published: (2018-12-01) -
Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant - Case report
by: Gabriela Maria Abreu Gontijo, et al.
Published: (2013-12-01) -
Case Report - Multinodular goiter in a patient with Congenital Hypothyroidism and Bannayan-Riley-Ruvalcaba syndrome: the possible synergic role of TPO and PTEN mutation
by: Gaia Vincenzi, et al.
Published: (2023-06-01)