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Yang, C. Acute Necrotizing Encephalopathy Type 1. Encyclopedia. Available online: https://encyclopedia.pub/entry/4456 (accessed on 27 September 2026).
Yang C. Acute Necrotizing Encephalopathy Type 1. Encyclopedia. Available at: https://encyclopedia.pub/entry/4456. Accessed September 27, 2026.
Yang, Catherine. "Acute Necrotizing Encephalopathy Type 1" Encyclopedia, https://encyclopedia.pub/entry/4456 (accessed September 27, 2026).
Yang, C. (2020, December 23). Acute Necrotizing Encephalopathy Type 1. In Encyclopedia. https://encyclopedia.pub/entry/4456
Yang, Catherine. "Acute Necrotizing Encephalopathy Type 1." Encyclopedia. Web. 23 December, 2020.
Acute Necrotizing Encephalopathy Type 1
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/acute-necrotizing-encephalopathy-type-1

Acute necrotizing encephalopathy type 1, also known as susceptibility to infection-induced acute encephalopathy 3 or IIAE3, is a rare type of brain disease (encephalopathy) that occurs following a viral infection such as the flu.

genetic conditions

References

  1. Bloch C, Suter B, Fischmann A, Gensicke H, Rüegg S, Weisser M. Only a Touch ofthe Flu? The Simultaneous Manifestation of Acute Necrotizing Encephalopathy inTwo Consanguineous Patients. Open Forum Infect Dis. 2015 Feb 2;2(2):ofv013. doi: 10.1093/ofid/ofv013.
  2. Neilson DE, Adams MD, Orr CM, Schelling DK, Eiben RM, Kerr DS, Anderson J,Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, Dohna-Schwake C,Dueckers G, Fasano AE, Gika AD, Gionnis D, Gorman MP, Grattan-Smith PJ,Hackenberg A, Kuster A, Lentschig MG, Lopez-Laso E, Marco EJ, Mastroyianni S,Perrier J, Schmitt-Mechelke T, Servidei S, Skardoutsou A, Uldall P, van der KnaapMS, Goglin KC, Tefft DL, Aubin C, de Jager P, Hafler D, Warman ML.Infection-triggered familial or recurrent cases of acute necrotizingencephalopathy caused by mutations in a component of the nuclear pore, RANBP2. AmJ Hum Genet. 2009 Jan;84(1):44-51. doi: 10.1016/j.ajhg.2008.12.009.
  3. Neilson DE. The interplay of infection and genetics in acute necrotizingencephalopathy. Curr Opin Pediatr. 2010 Dec;22(6):751-7. doi:10.1097/MOP.0b013e3283402bfe. Review.
  4. Sell K, Storch K, Hahn G, Lee-Kirsch MA, Ramantani G, Jackson S, Neilson D,von der Hagen M, Hehr U, Smitka M. Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation. Brain Dev. 2016Sep;38(8):777-80. doi: 10.1016/j.braindev.2016.02.007.
  5. Singh RR, Sedani S, Lim M, Wassmer E, Absoud M. RANBP2 mutation and acutenecrotizing encephalopathy: 2 cases and a literature review of the expandingclinico-radiological phenotype. Eur J Paediatr Neurol. 2015 Mar;19(2):106-13.doi: 10.1016/j.ejpn.2014.11.010.
  6. Wu X, Wu W, Pan W, Wu L, Liu K, Zhang HL. Acute necrotizing encephalopathy: anunderrecognized clinicoradiologic disorder. Mediators Inflamm. 2015;2015:792578. doi: 10.1155/2015/792578.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Catherine Yang
View Times: 906
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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