Literature DB >> 17880649

The treatment and management of alternating hemiplegia of childhood.

B G R Neville1, M Ninan.   

Abstract

Alternating hemiplegia of childhood has many factors that make it difficult to manage. These include its rarity of about one case per million, the variability of the manifestations, with seven characteristic features, and the potential for disabilities and acute, often severe, episodes in a disease that is of uncertain cause and for which treatment evidence is sparse. An integrated multidisciplinary team and emergency availability are key medical requirements, as well as an educational setting that understands the variations in performance that occur. The mainstays of treatment have been flunarizine, antiepilepsy drugs for the 50% of patients with epilepsy, attempts to avoid trigger situations, and the rapid encouragement of sleep when attacks begin. The diagnostic and management predicament of child, parent, and paediatrician in complex rare disorders are well illustrated by this condition.

Entities:  

Mesh:

Year:  2007        PMID: 17880649     DOI: 10.1111/j.1469-8749.2007.00777.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  26 in total

Review 1.  Pediatric migraine variants: a review of epidemiology, diagnosis, treatment, and outcome.

Authors:  Ana Marissa Lagman-Bartolome; Christine Lay
Journal:  Curr Neurol Neurosci Rep       Date:  2015-06       Impact factor: 5.081

Review 2.  Diagnosis and Treatment of Alternating Hemiplegia of Childhood.

Authors:  Melanie Masoud; Lyndsey Prange; Jeffrey Wuchich; Arsen Hunanyan; Mohamad A Mikati
Journal:  Curr Treat Options Neurol       Date:  2017-02       Impact factor: 3.598

Review 3.  The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.

Authors:  Matthew T Sweney; Tara M Newcomb; Kathryn J Swoboda
Journal:  Pediatr Neurol       Date:  2014-10-13       Impact factor: 3.372

Review 4.  Distinct neurological disorders with ATP1A3 mutations.

Authors:  Erin L Heinzen; Alexis Arzimanoglou; Allison Brashear; Steven J Clapcote; Fiorella Gurrieri; David B Goldstein; Sigurður H Jóhannesson; Mohamad A Mikati; Brian Neville; Sophie Nicole; Laurie J Ozelius; Hanne Poulsen; Tsveta Schyns; Kathleen J Sweadner; Arn van den Maagdenberg; Bente Vilsen
Journal:  Lancet Neurol       Date:  2014-05       Impact factor: 44.182

5.  Alternating Hemiplegia of Childhood: A Series of Genetically Confirmed Four Cases from Southern India with Review of Published Literature.

Authors:  Naveen Kumar Bhardwaj; Vykuntaraju K Gowda; Ashwin Vivek Sardesai
Journal:  J Pediatr Genet       Date:  2020-08-13

6.  Progressive Brain Atrophy in Alternating Hemiplegia of Childhood.

Authors:  Masayuki Sasaki; Atsushi Ishii; Yoshiaki Saito; Shinichi Hirose
Journal:  Mov Disord Clin Pract       Date:  2017-01-05

7.  De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.

Authors:  Erin L Heinzen; Kathryn J Swoboda; Yuki Hitomi; Fiorella Gurrieri; Sophie Nicole; Boukje de Vries; F Danilo Tiziano; Bertrand Fontaine; Nicole M Walley; Sinéad Heavin; Eleni Panagiotakaki; Stefania Fiori; Emanuela Abiusi; Lorena Di Pietro; Matthew T Sweney; Tara M Newcomb; Louis Viollet; Chad Huff; Lynn B Jorde; Sandra P Reyna; Kelley J Murphy; Kevin V Shianna; Curtis E Gumbs; Latasha Little; Kenneth Silver; Louis J Ptáček; Joost Haan; Michel D Ferrari; Ann M Bye; Geoffrey K Herkes; Charlotte M Whitelaw; David Webb; Bryan J Lynch; Peter Uldall; Mary D King; Ingrid E Scheffer; Giovanni Neri; Alexis Arzimanoglou; Arn M J M van den Maagdenberg; Sanjay M Sisodiya; Mohamad A Mikati; David B Goldstein
Journal:  Nat Genet       Date:  2012-07-29       Impact factor: 38.330

8.  Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.

Authors:  Greer S Kirshenbaum; Neil Dawson; Jonathan G L Mullins; Tom H Johnston; Mark J Drinkhill; Ian J Edwards; Susan H Fox; Judith A Pratt; Jonathan M Brotchie; John C Roder; Steven J Clapcote
Journal:  PLoS One       Date:  2013-03-20       Impact factor: 3.240

9.  Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients.

Authors:  Atsushi Ishii; Yoshiaki Saito; Jun Mitsui; Hiroyuki Ishiura; Jun Yoshimura; Hidee Arai; Sumimasa Yamashita; Sadami Kimura; Hirokazu Oguni; Shinichi Morishita; Shoji Tsuji; Masayuki Sasaki; Shinichi Hirose
Journal:  PLoS One       Date:  2013-02-08       Impact factor: 3.240

10.  Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation.

Authors:  Greer S Kirshenbaum; James Dachtler; John C Roder; Steven J Clapcote
Journal:  Behav Neurosci       Date:  2015-10-26       Impact factor: 1.912

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