Literature DB >> 31687261

Excessive Seizure Clusters in an Otherwise Well-Controlled Epilepsy as a Possible Hallmark of Untreated Vitamin B6-Responsive Epilepsy due to a Homozygous PLPBP Missense Variant.

Jessika Johannsen1, Tatjana Bierhals2, Philipp Deindl1, Laura Hecher1, Katharina Hermann1, Maja Hempel2, Katja Kloth2, Jonas Denecke1.   

Abstract

Recently, mutations in the PLPBP gene were described as a novel cause for vitamin B6-responsive epilepsy. We report the outcome in case of a male adolescent with a novel homozygous missense variant in PLPBP who was never treated with pyridoxine until the age of 16 years. He presented with only mild cognitive impairment and an early-onset, well-controlled epilepsy. In our patient, excessive seizure clusters and anxiety states occurred intermittently, suggesting that the combination might be a hallmark in untreated patients. Thus, mutations in PLPBP should be addressed even in adolescent patients with only mild learning disabilities and relatively good seizure control over the years. © Thieme Medical Publishers.

Entities:  

Keywords:  PLPBP (PROSC) gene; seizure cluster; vitamin B6 responsive epilepsy

Year:  2019        PMID: 31687261      PMCID: PMC6824897          DOI: 10.1055/s-0039-1685501

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  14 in total

1.  De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.

Authors:  Maja Hempel; Kirsten Cremer; Charlotte W Ockeloen; Klaske D Lichtenbelt; Johanna C Herkert; Jonas Denecke; Tobias B Haack; Alexander M Zink; Jessica Becker; Eva Wohlleber; Jessika Johannsen; Bader Alhaddad; Rolph Pfundt; Sigrid Fuchs; Dagmar Wieczorek; Tim M Strom; Koen L I van Gassen; Tjitske Kleefstra; Christian Kubisch; Hartmut Engels; Davor Lessel
Journal:  Am J Hum Genet       Date:  2015-09-03       Impact factor: 11.025

Review 2.  Neuroendocrinology of pyridoxine deficiency.

Authors:  K Dakshinamurti; C S Paulose; M Viswanathan; Y L Siow
Journal:  Neurosci Biobehav Rev       Date:  1988 Fall-Winter       Impact factor: 8.989

3.  Diagnostic clarity of exome sequencing following negative comprehensive panel testing in the neonatal intensive care unit.

Authors:  Kristin D Kernohan; Taila Hartley; Sergey Naumenko; Christine M Armour; Gail E Graham; Sarah M Nikkel; Matthew Lines; Michael T Geraghty; Julie Richer; Wendy Mears; Kym M Boycott; David A Dyment
Journal:  Am J Med Genet A       Date:  2018-07       Impact factor: 2.802

4.  REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.

Authors:  Nilah M Ioannidis; Joseph H Rothstein; Vikas Pejaver; Sumit Middha; Shannon K McDonnell; Saurabh Baheti; Anthony Musolf; Qing Li; Emily Holzinger; Danielle Karyadi; Lisa A Cannon-Albright; Craig C Teerlink; Janet L Stanford; William B Isaacs; Jianfeng Xu; Kathleen A Cooney; Ethan M Lange; Johanna Schleutker; John D Carpten; Isaac J Powell; Olivier Cussenot; Geraldine Cancel-Tassin; Graham G Giles; Robert J MacInnis; Christiane Maier; Chih-Lin Hsieh; Fredrik Wiklund; William J Catalona; William D Foulkes; Diptasri Mandal; Rosalind A Eeles; Zsofia Kote-Jarai; Carlos D Bustamante; Daniel J Schaid; Trevor Hastie; Elaine A Ostrander; Joan E Bailey-Wilson; Predrag Radivojac; Stephen N Thibodeau; Alice S Whittemore; Weiva Sieh
Journal:  Am J Hum Genet       Date:  2016-09-22       Impact factor: 11.025

5.  Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy.

Authors:  Niklas Darin; Emma Reid; Laurence Prunetti; Lena Samuelsson; Ralf A Husain; Matthew Wilson; Basma El Yacoubi; Emma Footitt; W K Chong; Louise C Wilson; Helen Prunty; Simon Pope; Simon Heales; Karine Lascelles; Mike Champion; Evangeline Wassmer; Pierangelo Veggiotti; Valérie de Crécy-Lagard; Philippa B Mills; Peter T Clayton
Journal:  Am J Hum Genet       Date:  2016-12-01       Impact factor: 11.025

6.  Confirmation of mutations in PROSC as a novel cause of vitamin B 6 -dependent epilepsy.

Authors:  Barbara Plecko; Markus Zweier; Anaïs Begemann; Deborah Mathis; Bernhard Schmitt; Pasquale Striano; Martina Baethmann; Maria Stella Vari; Francesca Beccaria; Federico Zara; Lisa M Crowther; Pascal Joset; Heinrich Sticht; Sorina Mihaela Papuc; Anita Rauch
Journal:  J Med Genet       Date:  2017-04-08       Impact factor: 6.318

7.  A method and server for predicting damaging missense mutations.

Authors:  Ivan A Adzhubei; Steffen Schmidt; Leonid Peshkin; Vasily E Ramensky; Anna Gerasimova; Peer Bork; Alexey S Kondrashov; Shamil R Sunyaev
Journal:  Nat Methods       Date:  2010-04       Impact factor: 28.547

8.  Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.

Authors:  Davor Lessel; Bruno Vaz; Swagata Halder; Paul J Lockhart; Ivana Marinovic-Terzic; Jaime Lopez-Mosqueda; Melanie Philipp; Joe C H Sim; Katherine R Smith; Judith Oehler; Elisa Cabrera; Raimundo Freire; Kate Pope; Amsha Nahid; Fiona Norris; Richard J Leventer; Martin B Delatycki; Gotthold Barbi; Simon von Ameln; Josef Högel; Marina Degoricija; Regina Fertig; Martin D Burkhalter; Kay Hofmann; Holger Thiele; Janine Altmüller; Gudrun Nürnberg; Peter Nürnberg; Melanie Bahlo; George M Martin; Cora M Aalfs; Junko Oshima; Janos Terzic; David J Amor; Ivan Dikic; Kristijan Ramadan; Christian Kubisch
Journal:  Nat Genet       Date:  2014-09-28       Impact factor: 38.330

9.  A general framework for estimating the relative pathogenicity of human genetic variants.

Authors:  Martin Kircher; Daniela M Witten; Preti Jain; Brian J O'Roak; Gregory M Cooper; Jay Shendure
Journal:  Nat Genet       Date:  2014-02-02       Impact factor: 38.330

10.  PLPBP mutations cause variable phenotypes of developmental and epileptic encephalopathy.

Authors:  Hiroshi Shiraku; Mitsuko Nakashima; Saoko Takeshita; Chai-Soon Khoo; Muzhirah Haniffa; Gaik-Siew Ch'ng; Kazuma Takada; Keisuke Nakajima; Masayasu Ohta; Tohru Okanishi; Sotaro Kanai; Ayataka Fujimoto; Hirotomo Saitsu; Naomichi Matsumoto; Mitsuhiro Kato
Journal:  Epilepsia Open       Date:  2018-11-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.