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Yang, C. Alternating Hemiplegia of Childhood. Encyclopedia. Available online: https://encyclopedia.pub/entry/4707 (accessed on 29 September 2026).
Yang C. Alternating Hemiplegia of Childhood. Encyclopedia. Available at: https://encyclopedia.pub/entry/4707. Accessed September 29, 2026.
Yang, Catherine. "Alternating Hemiplegia of Childhood" Encyclopedia, https://encyclopedia.pub/entry/4707 (accessed September 29, 2026).
Yang, C. (2020, December 24). Alternating Hemiplegia of Childhood. In Encyclopedia. https://encyclopedia.pub/entry/4707
Yang, Catherine. "Alternating Hemiplegia of Childhood." Encyclopedia. Web. 24 December, 2020.
Alternating Hemiplegia of Childhood
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/alternating-hemiplegia-of-childhood

Alternating hemiplegia of childhood is a neurological condition characterized by recurrent episodes of temporary paralysis, often affecting one side of the body (hemiplegia). During some episodes, the paralysis alternates from one side of the body to the other or affects both sides at the same time. These episodes begin in infancy or early childhood, usually before 18 months of age, and the paralysis lasts from minutes to days.

genetic conditions

References

  1. Bassi MT, Bresolin N, Tonelli A, Nazos K, Crippa F, Baschirotto C, Zucca C,Bersano A, Dolcetta D, Boneschi FM, Barone V, Casari G. A novel mutation in theATP1A2 gene causes alternating hemiplegia of childhood. J Med Genet. 2004Aug;41(8):621-8.
  2. Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, TizianoFD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E; European AlternatingHemiplegia of Childhood (AHC) Genetics Consortium; Biobanca e Registro Clinicoper l'Emiplegia Alternante (I.B.AHC) Consortium; European Network for Research onAlternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs)Consortium, Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L,Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM,Sisodiya SM, Mikati MA, Goldstein DB. De novo mutations in ATP1A3 causealternating hemiplegia of childhood. Nat Genet. 2012 Sep;44(9):1030-4. doi:10.1038/ng.2358.
  3. Panagiotakaki E, De Grandis E, Stagnaro M, Heinzen EL, Fons C, Sisodiya S, de Vries B, Goubau C, Weckhuysen S, Kemlink D, Scheffer I, Lesca G, Rabilloud M,Klich A, Ramirez-Camacho A, Ulate-Campos A, Campistol J, Giannotta M, Moutard ML,Doummar D, Hubsch-Bonneaud C, Jaffer F, Cross H, Gurrieri F, Tiziano D,Nevsimalova S, Nicole S, Neville B, van den Maagdenberg AM, Mikati M, GoldsteinDB, Vavassori R, Arzimanoglou A; Italian IBAHC Consortium; French AHC Consortium;International AHC Consortium. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet J RareDis. 2015 Sep 26;10:123. doi: 10.1186/s13023-015-0335-5.
  4. Rosewich H, Thiele H, Ohlenbusch A, Maschke U, Altmüller J, Frommolt P, ZirnB, Ebinger F, Siemes H, Nürnberg P, Brockmann K, Gärtner J. Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: awhole-exome sequencing gene-identification study. Lancet Neurol. 2012Sep;11(9):764-73. doi: 10.1016/S1474-4422(12)70182-5.
  5. Sweney MT, Silver K, Gerard-Blanluet M, Pedespan JM, Renault F, ArzimanoglouA, Schlesinger-Massart M, Lewelt AJ, Reyna SP, Swoboda KJ. Alternating hemiplegiaof childhood: early characteristics and evolution of a neurodevelopmentalsyndrome. Pediatrics. 2009 Mar;123(3):e534-41. doi: 10.1542/peds.2008-2027.
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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
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Entry Collection: MedlinePlus
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Update Date: 24 Dec 2020
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