Peutz–Jeghers syndrome: a multidisciplinary approach to diagnosis based on a clinical case-Reference-Cited by-同舟云学术

Peutz–Jeghers syndrome: a multidisciplinary approach to diagnosis based on a clinical case

Published:2022-01-20 Issue:4 Volume:8 Page:95-102
ISSN:2413-5496
Container-title:Russian Journal of Pediatric Hematology and Oncology
language:
Short-container-title:Ross. ž. det. gematol. onkol.

Author:

Belysheva T. S.¹^ORCID,Nasedkina T. V.²^ORCID,Valiev T. T.³^ORCID,Matinyan N. V.¹^ORCID,Malikhova O. A.³^ORCID,Semenova V. V.⁴^ORCID,Kozlova V. M.¹^ORCID,Kazubskaya T. P.¹^ORCID,Vishnevskaya Y. V.¹^ORCID,Mikhailova S. N.¹^ORCID,Varfolomeeva S. R.¹^ORCID

Affiliation:

1. N.N. Blokhin National Medical Research Centre of Oncology, Ministry of Health of Russia

2. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Health of Russia

3. N.N. Blokhin National Medical Research Centre of Oncology, Ministry of Health of Russia; Russian Medical Academy of Continuous Professional Education, Ministry of Health of Russia

4. N.N. Blokhin National Medical Research Centre of Oncology, Ministry of Health of Russia; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Health of Russia

Publisher

OOO Grafika

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference29 articles.

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3. Altamish M., Dahiya R., Singh A.K., Mishra A., Aljabali A.A.A., Satija S., Mehta M., Dureja H., Prasher P., Negi P., Kapoor D.N., Goyal R., Tambuwala M.M., Chellappan D.K., Dua K., Gupta G. Role of the Serine/Threonine Kinase 11 (STK11) or Liver Kinase B1 (LKB1) Gene in Peutz–Jeghers Syndrome. Crit Rev Eukaryot Gene Expr. 2020;30(3):245–52. doi:10.1615/CritRevEukaryotGeneExpr.2020033451. PMID:32749111.

4. Aretz S., Stienen D., Uhlhaas S., Loff S., Back W., Pagenstecher C., McLeod D.R., Graham G.E., Mangold E., Santer R., Propping P., Friedl W. High proportion of large genomic STK11 deletions in Peutz–Jeghers syndrome. Hum Mutat. 2005;26(6):513–9. doi:10.1002/humu.20253. PMID:16287113.

5. Zhao H.M., Yang Y.J., Duan J.Q., Ouyang H.J., Liu L., Yi L.C., Xiao Z.H., Zheng Y., Peng L., Attard T.M., Li D.Y., You J.Y. Clinical and Genetic Study of Children With Peutz–Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation. J Pediatr Gastroenterol Nutr. 2019;68(2):199–206. doi:10.1097/MPG.0000000000002166. PMID:30334930.

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