Literature DB >> 26340046

Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy.

Zianka Fallil1, Heath Pardoe1, Robert Bachman1, Benjamin Cunningham1, Isha Parulkar2, Catherine Shain2, Annapurna Poduri2, Robert Knowlton3, Ruben Kuzniecky4.   

Abstract

PURPOSE: Periventricular nodular heterotopia (PVNH) is a malformation of cortical development due to impaired neuronal migration resulting in the formation of nodular masses of neurons and glial cells in close proximity to the ventricular walls. We report the clinical characteristics of the largest case series of FLNA-negative patients with seizures and bilateral periventricular heterotopia.
METHODS: Participants were recruited through the Epilepsy Phenome/Genome Project (EPGP), a multicenter collaborative effort to collect detailed phenotypic data and DNA on a large number of individuals with epilepsy, including a cohort with symptomatic epilepsy related to PVNH. Included subjects had epilepsy, and MRI confirmed bilateral PVNH. Magnetic resonance imaging studies were visually and quantitatively reviewed to investigate the topographic extent of PVNH, symmetry, and laterality. KEY
FINDINGS: We analyzed data on 71 patients with bilateral PVNH. The incidence of febrile seizures was 16.6%. There was at least one other family member with epilepsy in 36.9% of this population. Developmental delay was present in 21.8%. Focal onset seizures were the most common type of seizure presentation (79.3%). High heterotopia burden was strongly associated with female gender and trigonal nodular localization. There was no evidence for differences in brain volume between PVNH subjects and controls. No relationship was observed between heterotopic volume and gender, developmental delay, location of PVNH, ventricular or cerebellar abnormalities, laterality of seizure onset, age at seizure onset, and duration of epilepsy. SIGNIFICANCE: A direct correlation was observed between high heterotopia burden, female gender, and trigonal location in this large cohort of FLNA-negative bilateral PVNH patients with epilepsy. Quantitative MRI measurements indicated that this correlation is based on the diffuse nature of the heterotopic nodules rather than on the total volume of abnormal heterotopic tissue.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Epilepsy; Epilepsy Phenome/Genome Project; Periventricular nodular heterotopia

Mesh:

Substances:

Year:  2015        PMID: 26340046      PMCID: PMC4594191          DOI: 10.1016/j.yebeh.2015.07.041

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  24 in total

1.  Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm.

Authors:  Y Zhang; M Brady; S Smith
Journal:  IEEE Trans Med Imaging       Date:  2001-01       Impact factor: 10.048

2.  Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.

Authors:  E Parrini; A Ramazzotti; W B Dobyns; D Mei; F Moro; P Veggiotti; C Marini; E H Brilstra; B Dalla Bernardina; L Goodwin; A Bodell; M C Jones; M Nangeroni; S Palmeri; E Said; J W Sander; P Striano; Y Takahashi; L Van Maldergem; G Leonardi; M Wright; C A Walsh; R Guerrini
Journal:  Brain       Date:  2006-05-09       Impact factor: 13.501

3.  Periventricular nodular heterotopia and intractable temporal lobe epilepsy: poor outcome after temporal lobe resection.

Authors:  L M Li; F Dubeau; F Andermann; D R Fish; C Watson; G D Cascino; S F Berkovic; N Moran; J S Duncan; A Olivier; R Leblanc; W Harkness
Journal:  Ann Neurol       Date:  1997-05       Impact factor: 10.422

4.  The clinical spectrum of nodular heterotopias in children: report of 31 patients.

Authors:  Myriam Srour; Marie-France Rioux; Caroline Varga; Anne Lortie; Philippe Major; Yves Robitaille; Jean-Claude Décarie; Jacques Michaud; Lionel Carmant
Journal:  Epilepsia       Date:  2011-02-14       Impact factor: 5.864

5.  The epilepsy phenome/genome project.

Authors:  Bassel Abou-Khalil; Brian Alldredge; Jocelyn Bautista; Sam Berkovic; Judith Bluvstein; Alex Boro; Gregory Cascino; Damian Consalvo; Sabrina Cristofaro; Patricia Crumrine; Orrin Devinsky; Dennis Dlugos; Michael Epstein; Robyn Fahlstrom; Miguel Fiol; Nathan Fountain; Kristen Fox; Jacqueline French; Catharine Freyer Karn; Daniel Friedman; Eric Geller; Tracy Glauser; Simon Glynn; Kevin Haas; Sheryl Haut; Jean Hayward; Sandra Helmers; Sucheta Joshi; Andres Kanner; Heidi Kirsch; Robert Knowlton; Eric Kossoff; Rachel Kuperman; Ruben Kuzniecky; Daniel Lowenstein; Shannon McGuire; Paul Motika; Gerard Nesbitt; Edward Novotny; Ruth Ottman; Juliann Paolicchi; Jack Parent; Kristen Park; Annapurna Poduri; Neil Risch; Lynette Sadleir; Ingrid Scheffer; Renee Shellhaas; Elliott Sherr; Jerry J Shih; Shlomo Shinnar; Rani Singh; Joseph Sirven; Michael Smith; Joe Sullivan; Liu Lin Thio; Anu Venkat; Eileen Vining; Gretchen von Allmen; Judith Weisenberg; Peter Widdess-Walsh; Melodie Winawer
Journal:  Clin Trials       Date:  2013-07-01       Impact factor: 2.486

6.  Filamin B mutations cause chondrocyte defects in skeletal development.

Authors:  Jie Lu; Gewei Lian; Robert Lenkinski; Alec De Grand; R Roy Vaid; Thomas Bryce; Marina Stasenko; Adele Boskey; Christopher Walsh; Volney Sheen
Journal:  Hum Mol Genet       Date:  2007-05-17       Impact factor: 6.150

7.  Periventricular and subcortical nodular heterotopia. A study of 33 patients.

Authors:  F Dubeau; D Tampieri; N Lee; E Andermann; S Carpenter; R Leblanc; A Olivier; R Radtke; J G Villemure; F Andermann
Journal:  Brain       Date:  1995-10       Impact factor: 13.501

8.  De novo mutations in epileptic encephalopathies.

Authors:  Andrew S Allen; Samuel F Berkovic; Patrick Cossette; Norman Delanty; Dennis Dlugos; Evan E Eichler; Michael P Epstein; Tracy Glauser; David B Goldstein; Yujun Han; Erin L Heinzen; Yuki Hitomi; Katherine B Howell; Michael R Johnson; Ruben Kuzniecky; Daniel H Lowenstein; Yi-Fan Lu; Maura R Z Madou; Anthony G Marson; Heather C Mefford; Sahar Esmaeeli Nieh; Terence J O'Brien; Ruth Ottman; Slavé Petrovski; Annapurna Poduri; Elizabeth K Ruzzo; Ingrid E Scheffer; Elliott H Sherr; Christopher J Yuskaitis; Bassel Abou-Khalil; Brian K Alldredge; Jocelyn F Bautista; Samuel F Berkovic; Alex Boro; Gregory D Cascino; Damian Consalvo; Patricia Crumrine; Orrin Devinsky; Dennis Dlugos; Michael P Epstein; Miguel Fiol; Nathan B Fountain; Jacqueline French; Daniel Friedman; Eric B Geller; Tracy Glauser; Simon Glynn; Sheryl R Haut; Jean Hayward; Sandra L Helmers; Sucheta Joshi; Andres Kanner; Heidi E Kirsch; Robert C Knowlton; Eric H Kossoff; Rachel Kuperman; Ruben Kuzniecky; Daniel H Lowenstein; Shannon M McGuire; Paul V Motika; Edward J Novotny; Ruth Ottman; Juliann M Paolicchi; Jack M Parent; Kristen Park; Annapurna Poduri; Ingrid E Scheffer; Renée A Shellhaas; Elliott H Sherr; Jerry J Shih; Rani Singh; Joseph Sirven; Michael C Smith; Joseph Sullivan; Liu Lin Thio; Anu Venkat; Eileen P G Vining; Gretchen K Von Allmen; Judith L Weisenberg; Peter Widdess-Walsh; Melodie R Winawer
Journal:  Nature       Date:  2013-08-11       Impact factor: 49.962

Review 9.  Familial history and recurrence of febrile seizures; a systematic review and meta-analysis.

Authors:  Yousef Veisani; Ali Delpisheh; Kourosh Sayehmiri
Journal:  Iran J Pediatr       Date:  2013-08       Impact factor: 0.364

10.  The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.

Authors:  A Di Martino; C-G Yan; Q Li; E Denio; F X Castellanos; K Alaerts; J S Anderson; M Assaf; S Y Bookheimer; M Dapretto; B Deen; S Delmonte; I Dinstein; B Ertl-Wagner; D A Fair; L Gallagher; D P Kennedy; C L Keown; C Keysers; J E Lainhart; C Lord; B Luna; V Menon; N J Minshew; C S Monk; S Mueller; R-A Müller; M B Nebel; J T Nigg; K O'Hearn; K A Pelphrey; S J Peltier; J D Rudie; S Sunaert; M Thioux; J M Tyszka; L Q Uddin; J S Verhoeven; N Wenderoth; J L Wiggins; S H Mostofsky; M P Milham
Journal:  Mol Psychiatry       Date:  2013-06-18       Impact factor: 15.992

View more
  4 in total

1.  De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.

Authors:  Erin L Heinzen; Adam C O'Neill; Xiaolin Zhu; Andrew S Allen; Melanie Bahlo; Jamel Chelly; Ming Hui Chen; William B Dobyns; Saskia Freytag; Renzo Guerrini; Richard J Leventer; Annapurna Poduri; Stephen P Robertson; Christopher A Walsh; Mengqi Zhang
Journal:  PLoS Genet       Date:  2018-05-08       Impact factor: 5.917

2.  Size of Subcortical Band Heterotopia Influences the Susceptibility to Hyperthermia-Induced Seizures in a Rat Model.

Authors:  Kalliopi Moustaki; Emmanuelle Buhler; Robert Martinez; Françoise Watrin; Alfonso Represa; Jean-Bernard Manent
Journal:  Front Cell Neurosci       Date:  2019-10-18       Impact factor: 5.505

3.  The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia.

Authors:  Yan-Ting Lu; Chung-Yao Hsu; Yo-Tsen Liu; Chung-Kin Chan; Yao-Chung Chuang; Chih-Hsiang Lin; Kai-Ping Chang; Chen-Jui Ho; Ching-Ching Ng; Kheng-Seang Lim; Meng-Han Tsai
Journal:  Biomed J       Date:  2021-05-20       Impact factor: 7.892

4.  Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation.

Authors:  Xiaoyan Ge; Henry Gong; Kevin Dumas; Jessica Litwin; Joanna J Phillips; Quinten Waisfisz; Marjan M Weiss; Yvonne Hendriks; Kyra E Stuurman; Stanley F Nelson; Wayne W Grody; Hane Lee; Pui-Yan Kwok; Joseph Tc Shieh
Journal:  NPJ Genom Med       Date:  2016-10-05       Impact factor: 8.617

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.