Neonatal Diabetes Mellitus in the Structure of IPEX Syndrome
- 作者: Turkunova M.E1, Ditkovskaya L.V1, Suspitsin E.N1, Tyrtova L.V1, Jelenina L.A1, Guseva M.N1
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隶属关系:
- St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
- 期: 卷 8, 编号 2 (2017)
- 页面: 99-104
- 栏目: Articles
- URL: https://journals.rcsi.science/pediatr/article/view/6423
- DOI: https://doi.org/10.17816/PED8299-104
- ID: 6423
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作者简介
Mariia Turkunova
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: 89650505452@mail.ru
Postgraduate Student, Department of Pediatrics, Endocrinology and Abilitology, Faculty of Postgraduate Education Saint Petersburg, Russia
Liliya Ditkovskaya
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: liliya-ditkovskaya@yandex.ru
MD, PhD, Associate Professor, Department of Pediatrics, Endocrinology and Abilitology, Faculty of Postgraduate Education Saint Petersburg, Russia
Evgenii Suspitsin
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: suspitsin@hotmail.ru
MD, PhD, Associate Professor, Department of Medicine Genetic Saint Petersburg, Russia
Ludmila Tyrtova
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: dr-tyrtova@yandex.ru
MD, PhD, Dr Med Sci, Professor, Head, A.F. Tur Department of policlinic therapy Saint Petersburg, Russia
Ludmila Jelenina
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: jelenina@mail.ru
MD, PhD, Dr Med Sci, Professor, Head, Department of Pediatrics, Endocrinology and Abilitology, Faculty of Postgraduate Education Saint Petersburg, Russia
Marina Guseva
St Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation
Email: gusevamarina@mail.ru
MD, Allergy-Immunologist, Consutative and Diagnostic centre Saint Petersburg, Russia
参考
- Иванов Д.О. Нарушения обмена глюкозы у новорожденных // Детская медицина Северо-Запада. - 2011. - Т. 2. - № 1. - С. 68-91.
- Никитина И.Л., Скородок Ю.Л., Дитковская Л.В., Гринева Е.Н. Сахарный диабет у детей и подростков: Учебное пособие. - СПб., 2010.
- Тихонович Ю.В., Петряйкина Е.Е., Рыбкина И.Г., и др. Х-сцепленные иммунная дисрегуляция, полиэндокринопатия и энтеропатия (IPEX-синдром): описание клинического случая и краткий обзор литературы // Проблемы эндокринологии. - 2014. - № 5. - С. 29-33.
- Bacchetta R, Barzaghi F, Roncarolo Maria-Grazia. From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation. Ann NY Acad Sci. 2016;1-18. doi: 10.1111/nyas.13011.
- Bennett CL, Christie J, Ramsdell F, et al. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat Genet. 2001;27(1):20-21.
- Bindl L, Torgerson T, Perroni L, et al. Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome). J Pediatr. 2005;147(2):256-9.
- Bis S, Maguiness SM, Gellis SE, et al. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome associated with neonatal epidermolysis bullosa acquisita. Pediatr Dermatol. 2015;32: e74-77.
- Bousfiha A, Jeddane L, Al-Herz W, et al. The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies. J Clin Immunol. 2015;35:727-738. doi: 10.1007/s10875-015-0198-5.
- De Benedetti F, Insalaco A, Diamanti A, et al. Mechanistic associations of a mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome. Clin Gastroenterol Hepatol. 2006;(4):653-659.
- Chatila TA, Blaeser F, Ho N, et al. JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome. J Clin Invest. 2000;106(12): R75-81.
- Horino S, Sasahara Y, Sato M, et al. Selective expansion of donor-derived regulatory T-cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome. Pediatr Transplantation. 2014;(18): E25-E30.
- Lampasona V, Passerini L, Barzaghi F, et al. Autoantibodies to harmonin and villin are diagnostic markers in children with IPEX syndrome. PLoS ONE. 2013. doi: 10.1371/journal.pone.0078664 (accessed 01.09.2016).
- Martín-Santiago A, Hervás JA, Hervás D, et al. Diagnostic value of the skin lesions in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. Pediatr Dermatol. 2013;30(6): e221-2.
- Moraes M, Da-Silva X, http://www.sciencedirect.com/science/article/pii/S152166161400285X - af0005 Moreira-Filho Carlos A, http://www.sciencedirect.com/science/article/pii/S152166161400285X - af0010 et al. http://www.sciencedirect.com/science/article/pii/S152166161400285X - af0010. Fetal-onset IPEX: Report of two families and review of literature. Clinical Immunology. 2015;156(2):131-140.
- Pagon RA, Adam MP, Ardinger HH, et al. A service of the National Library of Medicine, National Institutes of Health. Gene Reviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
- Powell BR, Buist NR, Stenzel P. An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy. J Pediatr. 1982;100(5):731-737.
- Rae W, http://www.sciencedirect.com/science/article/pii/S1521661615300395 - af0005 Gao Y, Bunyan D, http://www.sciencedirect.com/science/article/pii/S1521661615300395 - af0015 et al. A novel FOXP3 mutation causing fetal akinesia and recurrent male miscarriages. Clinical Immunology. 2015;161(2):284-285.
- Rubio-Cabezas O, Minton JAL, Caswell R, et al. Clinical Heterogeneity in Patients With FOXP3 Mutations Presenting With Permanent Neonatal Diabetes. Diabetes Care. 2009;32(1):111-116.
- Reichert Sara L, McKay Eileen M, Moldenhauer Julie S. Identification of a Novel Nonsense Mutation in the FOXP3 Gene in a Fetus with Hydrops - Expanding the Phenotype of IPEX Syndrome. American Journal of Medical Genetics. PART A. 2015;226-232.
- Tsuda M, Torgerson TR, Selmi C, et al. The spectrum of autoantibodies in IPEX syndrome is broad and includes antimitochondrial autoantibodies. J Autoimmun. 2010;35(3):265-268.
- Wildin RS, Ramsdell F, Peake J, et al. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nat Genet. 2001;27(1):18-20.
- Yong PL, Russo P, Sullivan KE. Use of sirolimus in IPEX and IPEX-like children. J Clin Immunol. 2008;28(5):581-7.
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