Literature DB >> 27343026

PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies.

Pawel Gawlinski1, Renata Posmyk2, Tomasz Gambin3, Danuta Sielicka4, Monika Chorazy5, Beata Nowakowska1, Shalini N Jhangiani6, Donna M Muzny6, Monika Bekiesinska-Figatowska7, Jerzy Bal1, Eric Boerwinkle8, Richard A Gibbs6, James R Lupski9, Wojciech Wiszniewski10.   

Abstract

BACKGROUND: Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO) syndrome is a distinct neurodevelopmental disorder. Patients without optic nerve atrophy and brain imaging abnormalities but fulfilling other PEHO criteria are often described as a PEHO-like syndrome. The molecular bases of both clinically defined conditions remain unknown in spite of the widespread application of genome analyses in both clinic and research.
METHODS: We enrolled two patients with a prior diagnosis of PEHO and two individuals with PEHO-like syndrome. All four individuals subsequently underwent whole-exome sequencing and comprehensive genomic analysis.
RESULTS: We identified disease-causing mutations in known genes associated with neurodevelopmental disorders including GNAO1 and CDKL5 in two of four individuals. One patient with PEHO syndrome and a de novoGNAO1 mutation was found to have an additional de novo mutation in HESX1 that is associated with optic atrophy.
CONCLUSIONS: We hypothesize that PEHO and PEHO-like syndrome may represent a severe end of the spectrum of the early-onset encephalopathies and, in some instances, its complex phenotype may result from an aggregated effect of mutations at two loci.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  PEHO; encephalopathy; neurodevelopmental disorder; optic atrophy; whole-exome sequencing

Mesh:

Substances:

Year:  2016        PMID: 27343026      PMCID: PMC5125779          DOI: 10.1016/j.pediatrneurol.2016.03.011

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  19 in total

Review 1.  The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.

Authors:  Jessica X Chong; Kati J Buckingham; Shalini N Jhangiani; Corinne Boehm; Nara Sobreira; Joshua D Smith; Tanya M Harrell; Margaret J McMillin; Wojciech Wiszniewski; Tomasz Gambin; Zeynep H Coban Akdemir; Kimberly Doheny; Alan F Scott; Dimitri Avramopoulos; Aravinda Chakravarti; Julie Hoover-Fong; Debra Mathews; P Dane Witmer; Hua Ling; Kurt Hetrick; Lee Watkins; Karynne E Patterson; Frederic Reinier; Elizabeth Blue; Donna Muzny; Martin Kircher; Kaya Bilguvar; Francesc López-Giráldez; V Reid Sutton; Holly K Tabor; Suzanne M Leal; Murat Gunel; Shrikant Mane; Richard A Gibbs; Eric Boerwinkle; Ada Hamosh; Jay Shendure; James R Lupski; Richard P Lifton; David Valle; Deborah A Nickerson; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2015-07-09       Impact factor: 11.025

2.  Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

Authors:  P Q Thomas; M T Dattani; J M Brickman; D McNay; G Warne; M Zacharin; F Cameron; J Hurst; K Woods; D Dunger; R Stanhope; S Forrest; I C Robinson; R S Beddington
Journal:  Hum Mol Genet       Date:  2001-01-01       Impact factor: 6.150

3.  Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in males.

Authors:  Julien Masliah-Plachon; Stéphane Auvin; Juliette Nectoux; Yann Fichou; Jamel Chelly; Thierry Bienvenu
Journal:  Am J Med Genet A       Date:  2010-08       Impact factor: 2.802

4.  Precocious puberty in two girls with PEHO syndrome: a clinical feature not previously described.

Authors:  Majid Alfadhel; Siu Li Yong; Yolanda Lillquist; Sylvie Langlois
Journal:  J Child Neurol       Date:  2011-05-18       Impact factor: 1.987

5.  Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

Authors:  Linda S Weaving; John Christodoulou; Sarah L Williamson; Kathie L Friend; Olivia L D McKenzie; Hayley Archer; Julie Evans; Angus Clarke; Gregory J Pelka; Patrick P L Tam; Catherine Watson; Hooshang Lahooti; Carolyn J Ellaway; Bruce Bennetts; Helen Leonard; Jozef Gécz
Journal:  Am J Hum Genet       Date:  2004-10-18       Impact factor: 11.025

Review 6.  The PEHO syndrome.

Authors:  R Riikonen
Journal:  Brain Dev       Date:  2001-11       Impact factor: 1.961

7.  Molecular findings among patients referred for clinical whole-exome sequencing.

Authors:  Yaping Yang; Donna M Muzny; Fan Xia; Zhiyv Niu; Richard Person; Yan Ding; Patricia Ward; Alicia Braxton; Min Wang; Christian Buhay; Narayanan Veeraraghavan; Alicia Hawes; Theodore Chiang; Magalie Leduc; Joke Beuten; Jing Zhang; Weimin He; Jennifer Scull; Alecia Willis; Megan Landsverk; William J Craigen; Mir Reza Bekheirnia; Asbjorg Stray-Pedersen; Pengfei Liu; Shu Wen; Wendy Alcaraz; Hong Cui; Magdalena Walkiewicz; Jeffrey Reid; Matthew Bainbridge; Ankita Patel; Eric Boerwinkle; Arthur L Beaudet; James R Lupski; Sharon E Plon; Richard A Gibbs; Christine M Eng
Journal:  JAMA       Date:  2014-11-12       Impact factor: 56.272

8.  Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO) syndrome in a Swiss child.

Authors:  Andrea Klein; Bernhard Schmitt; Eugen Boltshauser
Journal:  Eur J Paediatr Neurol       Date:  2004       Impact factor: 3.140

9.  Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.

Authors:  Matthew N Bainbridge; Min Wang; Yuanqing Wu; Irene Newsham; Donna M Muzny; John L Jefferies; Thomas J Albert; Daniel L Burgess; Richard A Gibbs
Journal:  Genome Biol       Date:  2011-07-25       Impact factor: 13.583

10.  Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region.

Authors:  E Montini; G Andolfi; A Caruso; G Buchner; S M Walpole; M Mariani; G Consalez; D Trump; A Ballabio; B Franco
Journal:  Genomics       Date:  1998-08-01       Impact factor: 5.736

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  9 in total

1.  PEHO syndrome caused by compound heterozygote variants in ZNHIT3 gene.

Authors:  Katrin Õunap; Kai Muru; Eve Õiglane-Shlik; Pilvi Ilves; Sander Pajusalu; Imbi Kuus; Monica H Wojcik; Tiia Reimand
Journal:  Eur J Med Genet       Date:  2019-04-29       Impact factor: 2.708

2.  Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.

Authors:  McKenna Kelly; Meredith Park; Ivana Mihalek; Anne Rochtus; Marie Gramm; Eduardo Pérez-Palma; Erika Takle Axeen; Christina Y Hung; Heather Olson; Lindsay Swanson; Irina Anselm; Lauren C Briere; Frances A High; David A Sweetser; Saima Kayani; Molly Snyder; Sophie Calvert; Ingrid E Scheffer; Edward Yang; Jeff L Waugh; Dennis Lal; Olaf Bodamer; Annapurna Poduri
Journal:  Epilepsia       Date:  2019-01-25       Impact factor: 5.864

3.  Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing.

Authors:  Theodora U J Bruun; Caro-Lyne DesRoches; Diane Wilson; Vann Chau; Tadashi Nakagawa; Masahiro Yamasaki; Shinya Hasegawa; Toshiyuki Fukao; Christian Marshall; Saadet Mercimek-Andrews
Journal:  Genet Med       Date:  2017-08-17       Impact factor: 8.822

4.  PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.

Authors:  Massimo Zollo; Mustafa Ahmed; Veronica Ferrucci; Vincenzo Salpietro; Fatemeh Asadzadeh; Marianeve Carotenuto; Reza Maroofian; Ahmed Al-Amri; Royana Singh; Iolanda Scognamiglio; Majid Mojarrad; Luca Musella; Angela Duilio; Angela Di Somma; Ender Karaca; Anna Rajab; Aisha Al-Khayat; Tribhuvan Mohan Mohapatra; Atieh Eslahi; Farah Ashrafzadeh; Lettie E Rawlins; Rajniti Prasad; Rashmi Gupta; Preeti Kumari; Mona Srivastava; Flora Cozzolino; Sunil Kumar Rai; Maria Monti; Gaurav V Harlalka; Michael A Simpson; Philip Rich; Fatema Al-Salmi; Michael A Patton; Barry A Chioza; Stephanie Efthymiou; Francesca Granata; Gabriella Di Rosa; Sarah Wiethoff; Eugenia Borgione; Carmela Scuderi; Kshitij Mankad; Michael G Hanna; Piero Pucci; Henry Houlden; James R Lupski; Andrew H Crosby; Emma L Baple
Journal:  Brain       Date:  2017-04-01       Impact factor: 13.501

5.  GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.

Authors:  Federica Rachele Danti; Serena Galosi; Marta Romani; Martino Montomoli; Keren J Carss; F Lucy Raymond; Elena Parrini; Claudia Bianchini; Tony McShane; Russell C Dale; Shekeeb S Mohammad; Ubaid Shah; Neil Mahant; Joanne Ng; Amy McTague; Rajib Samanta; Gayatri Vadlamani; Enza Maria Valente; Vincenzo Leuzzi; Manju A Kurian; Renzo Guerrini
Journal:  Neurol Genet       Date:  2017-03-21

6.  May PEHO Syndrome be a Clinical Entity Associated with Early Onset Encephalopathies?

Authors:  Arzu Ekici; İlyas Yılmaz; Orhan Görükmez; Cengiz Gökhan Orcan; Sevil Dorum
Journal:  Ann Indian Acad Neurol       Date:  2020-06-10       Impact factor: 1.383

7.  Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis.

Authors:  Soo Yeon Kim; YoungKyu Shim; Young Joon Ko; Soojin Park; Se Song Jang; Byung Chan Lim; Ki Joong Kim; Jong-Hee Chae
Journal:  Orphanet J Rare Dis       Date:  2020-12-09       Impact factor: 4.123

8.  The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.

Authors:  Vincenzo Salpietro; Massimo Zollo; Jana Vandrovcova; Mina Ryten; Juan A Botia; Veronica Ferrucci; Andreea Manole; Stephanie Efthymiou; Fuad Al Mutairi; Enrico Bertini; Marco Tartaglia; Henry Houlden
Journal:  Brain       Date:  2017-08-01       Impact factor: 13.501

9.  Mouse models of GNAO1-associated movement disorder: Allele- and sex-specific differences in phenotypes.

Authors:  Huijie Feng; Casandra L Larrivee; Elena Y Demireva; Huirong Xie; Jeff R Leipprandt; Richard R Neubig
Journal:  PLoS One       Date:  2019-01-25       Impact factor: 3.240

  9 in total

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