Literature DB >> 27629772

KCTD7-related progressive myoclonus epilepsy.

Patrick Van Bogaert1.   

Abstract

Progressive myoclonic epilepsy associated with KCTD7 mutations has been reported in 19 patients from 12 families. Patients show homozygous mutations in the coding regions of the KCTD7 gene. The disease starts in infancy. Patients typically show an initial severe epileptic disorder, with abundant epileptiform discharges on EEG and myoclonic seizures in the foreground, associated with cognitive regression and ataxia. Continuous multifocal myoclonus aggravated by action is observed in more than half of the cases. After a few years, the disease tends to stabilize and long survival can be expected. Some patients remain able to walk independently. The severity of the disease is variable from one patient to another, even within the same family. It is hypothesized that the epileptic disorder may influence the neurological regression observed in patients.

Entities:  

Keywords:  KCTD7; encephalopathy; infancy; progressive myoclonus epilepsies

Mesh:

Substances:

Year:  2016        PMID: 27629772     DOI: 10.1684/epd.2016.0856

Source DB:  PubMed          Journal:  Epileptic Disord        ISSN: 1294-9361            Impact factor:   1.819


  7 in total

1.  Progressive myoclonic epilepsy-associated gene Kctd7 regulates retinal neurovascular patterning and function.

Authors:  Jonathan Alevy; Courtney A Burger; Nicholas E Albrecht; Danye Jiang; Melanie A Samuel
Journal:  Neurochem Int       Date:  2019-06-06       Impact factor: 3.921

Review 2.  The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy.

Authors:  Alessandro Orsini; Angelo Valetto; Veronica Bertini; Mariagrazia Esposito; Niccolò Carli; Berge A Minassian; Alice Bonuccelli; Diego Peroni; Roberto Michelucci; Pasquale Striano
Journal:  Seizure       Date:  2019-08-23       Impact factor: 3.184

Review 3.  KCTD7-related progressive myoclonic epilepsy: report of three Indian families and review of literature.

Authors:  Dhanya Lakshmi Narayanan; Puneeth H Somashekar; Purvi Majethia; Anju Shukla
Journal:  Clin Dysmorphol       Date:  2022-01-01       Impact factor: 0.816

4.  The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patients.

Authors:  Filippo Pinto Vairo; Nicole J Boczek; Margot A Cousin; Charu Kaiwar; Patrick R Blackburn; Erin Conboy; Brendan C Lanpher; Ralitza H Gavrilova; Pavel N Pichurin; Konstantinos N Lazaridis; Dusica Babovic-Vuksanovic; Eric W Klee
Journal:  Mol Genet Metab Rep       Date:  2017-08-11

5.  Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.

Authors:  Giovanni Smaldone; Nicole Balasco; Luciano Pirone; Daniela Caruso; Sonia Di Gaetano; Emilia Maria Pedone; Luigi Vitagliano
Journal:  Sci Rep       Date:  2019-07-19       Impact factor: 4.379

6.  Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects.

Authors:  Justine H Liang; Jonathan Alevy; Viktor Akhanov; Ryan Seo; Cory A Massey; Danye Jiang; Joy Zhou; Roy V Sillitoe; Jeffrey L Noebels; Melanie A Samuel
Journal:  Dis Model Mech       Date:  2022-09-13       Impact factor: 5.732

Review 7.  Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force.

Authors:  Sterre van der Veen; Rodi Zutt; Christine Klein; Connie Marras; Samuel F Berkovic; John N Caviness; Hiroshi Shibasaki; Tom J de Koning; Marina A J Tijssen
Journal:  Mov Disord       Date:  2019-10-04       Impact factor: 10.338

  7 in total

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