Literature DB >> 31484714

The epileptology of alternating hemiplegia of childhood.

Julie Uchitel1, Ashley Helseth1, Lyndsey Prange1, Melissa McLean1, Ryan Ghusayni1, Monisha Sachdev1, Arsen Hunanyan1, Mohamad A Mikati2.   

Abstract

OBJECTIVE: To report our experience and investigate 5 original hypotheses: (1) multiple types of epileptic seizures occur in alternating hemiplegia of childhood (AHC), and these can be the initial presentation; (2) epileptiform abnormalities often appear well after clinical seizures; (3) nonepileptic reduced awareness spells (RAS) occur frequently; (4) epilepsy is commonly drug resistant but may respond to vagal nerve stimulation (VNS); and (5) status epilepticus (SE) is common and is usually refractory and recurrent.
METHODS: We analyzed a cohort of 51 consecutive patients with AHC.
RESULTS: Thirty-two of 51 patients had epilepsy: 18 focal seizures, frontal more frequently than temporal, and then posterior. Eleven had primary generalized seizures (tonic-clonic, myoclonic, and/or absence). Epileptic seizures preceded other AHC paroxysmal events in 8 (lag 5.63 ± 6.55 months; p = 0.0365). In 7 of 32, initial EEGs were normal, with the first epileptiform EEG lagging behind by 3.53 ± 4.65 years (p = 0.0484). RAS occurred equally in patients with epilepsy (16 of 32) and patients without epilepsy (10 of 19, p = 1.0). Twenty-eight patients had video-EEG; captured RAS showed no concomitant EEG changes. Nineteen patients (59%) were drug resistant. VNS resulted in >50% reduction in seizures in 5 of 6 (p < 0.04). Twelve patients (38%) had SE (9 of 12 multiple episodes), refractory/superrefractory in all (p < 0.001), and 4 of 12 had regression after SE.
CONCLUSIONS: Epilepsy in AHC can be focal or generalized. Epileptic seizures may be the first paroxysmal symptom. EEG may become epileptiform only on follow-up. Epilepsy, although frequently drug resistant, can respond to VNS. RAS are frequent and nonepileptic. SE often recurs and is usually refractory/superrefractory. Our observations are consistent with current data on AHC-ATP1A3 pathophysiology.
© 2019 American Academy of Neurology.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 31484714     DOI: 10.1212/WNL.0000000000008159

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  13 in total

1.  D-DEMØ, a distinct phenotype caused by ATP1A3 mutations.

Authors:  Lyndsey Prange; Milton Pratt; Kristin Herman; Raphael Schiffmann; David M Mueller; Melissa McLean; Mary Moya Mendez; Nicole Walley; Erin L Heinzen; David Goldstein; Vandana Shashi; Arsen Hunanyan; Vijay Pagadala; Mohamad A Mikati
Journal:  Neurol Genet       Date:  2020-08-04

2.  Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3Mashl/+, Mouse Model of Alternating Hemiplegia of Childhood.

Authors:  Arsen S Hunanyan; Boris Kantor; Ram S Puranam; Courtney Elliott; Angela McCall; Justin Dhindsa; Promila Pagadala; Keri Wallace; Jordan Poe; Talha Gunduz; Aravind Asokan; Dwight D Koeberl; Mai K ElMallah; Mohamad A Mikati
Journal:  Hum Gene Ther       Date:  2021-02-12       Impact factor: 5.695

3.  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

4.  Alternating Hemiplegia of Childhood: gastrointestinal manifestations and correlation with neurological impairments.

Authors:  Milton Pratt; Julie Uchitel; Nancy McGreal; Kelly Gordon; Lyndsey Prange; Melissa McLean; Richard J Noel; Blaire Rikard; Mary K Rogers Boruta; Mohamad A Mikati
Journal:  Orphanet J Rare Dis       Date:  2020-09-03       Impact factor: 4.123

5.  Decreased content of ascorbic acid (vitamin C) in the brain of knockout mouse models of Na+,K+-ATPase-related neurologic disorders.

Authors:  Keiko Ikeda; Adriana A Tienda; Fiona E Harrison; Kiyoshi Kawakami
Journal:  PLoS One       Date:  2021-02-05       Impact factor: 3.240

6.  De novo ATP1A3 variants cause polymicrogyria.

Authors:  Satoko Miyatake; Mitsuhiro Kato; Takuma Kumamoto; Tomonori Hirose; Eriko Koshimizu; Takaaki Matsui; Hideyuki Takeuchi; Hiroshi Doi; Keisuke Hamada; Mitsuko Nakashima; Kazunori Sasaki; Akio Yamashita; Atsushi Takata; Kohei Hamanaka; Mai Satoh; Takabumi Miyama; Yuri Sonoda; Momoko Sasazuki; Hiroyuki Torisu; Toshiro Hara; Yasunari Sakai; Yushi Noguchi; Mazumi Miura; Yoko Nishimura; Kazuyuki Nakamura; Hideyuki Asai; Nodoka Hinokuma; Fuyuki Miya; Tatsuhiko Tsunoda; Masami Togawa; Yukihiro Ikeda; Nobusuke Kimura; Kaoru Amemiya; Asako Horino; Masataka Fukuoka; Hiroko Ikeda; Goni Merhav; Nina Ekhilevitch; Masaki Miura; Takeshi Mizuguchi; Noriko Miyake; Atsushi Suzuki; Shouichi Ohga; Hirotomo Saitsu; Hidehisa Takahashi; Fumiaki Tanaka; Kazuhiro Ogata; Chiaki Ohtaka-Maruyama; Naomichi Matsumoto
Journal:  Sci Adv       Date:  2021-03-24       Impact factor: 14.136

7.  Genetically altered animal models for ATP1A3-related disorders.

Authors:  Hannah W Y Ng; Jennifer A Ogbeta; Steven J Clapcote
Journal:  Dis Model Mech       Date:  2021-10-06       Impact factor: 5.732

8.  Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability.

Authors:  Piero Pavone; Xena Giada Pappalardo; Naira Mustafa; Sung Yoon Cho; Dong Kyu Jin; Gemma Incorpora; Raffaele Falsaperla; Simona Domenica Marino; Giovanni Corsello; Enrico Parano; Martino Ruggieri
Journal:  Ital J Pediatr       Date:  2022-02-17       Impact factor: 2.638

9.  Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood.

Authors:  Marco Perulli; Josephine Poole; Giulia Di Lazzaro; Sasha D'Ambrosio; Katri Silvennoinen; Sara Zagaglia; Diego Jiménez-Jiménez; Domenica Battaglia; Sanjay M Sisodiya; Simona Balestrini
Journal:  Mov Disord Clin Pract       Date:  2021-12-29

10.  Early role for a Na+,K+-ATPase (ATP1A3) in brain development.

Authors:  Richard S Smith; Marta Florio; Shyam K Akula; Jennifer E Neil; Yidi Wang; R Sean Hill; Melissa Goldman; Christopher D Mullally; Nora Reed; Luis Bello-Espinosa; Laura Flores-Sarnat; Fabiola Paoli Monteiro; Casella B Erasmo; Filippo Pinto E Vairo; Eva Morava; A James Barkovich; Joseph Gonzalez-Heydrich; Catherine A Brownstein; Steven A McCarroll; Christopher A Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2021-06-22       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.