Literature DB >> 29724491

Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP.

Anke Van Dijck1, Anneke T Vulto-van Silfhout2, Elisa Cappuyns3, Ilse M van der Werf3, Grazia M Mancini4, Andreas Tzschach5, Raphael Bernier6, Illana Gozes7, Evan E Eichler8, Corrado Romano9, Anna Lindstrand10, Ann Nordgren10, Malin Kvarnung10, Tjitske Kleefstra2, Bert B A de Vries2, Sébastien Küry11, Jill A Rosenfeld12, Marije E Meuwissen3, Geert Vandeweyer3, R Frank Kooy3.   

Abstract

BACKGROUND: In genome-wide screening studies for de novo mutations underlying autism and intellectual disability, mutations in the ADNP gene are consistently reported among the most frequent. ADNP mutations have been identified in children with autism spectrum disorder comorbid with intellectual disability, distinctive facial features, and deficits in multiple organ systems. However, a comprehensive clinical description of the Helsmoortel-Van der Aa syndrome is lacking.
METHODS: We identified a worldwide cohort of 78 individuals with likely disruptive mutations in ADNP from January 2014 to October 2016 through systematic literature search, by contacting collaborators, and through direct interaction with parents. Clinicians filled in a structured questionnaire on genetic and clinical findings to enable correlations between genotype and phenotype. Clinical photographs and specialist reports were gathered. Parents were interviewed to complement the written questionnaires.
RESULTS: We report on the detailed clinical characterization of a large cohort of individuals with an ADNP mutation and demonstrate a distinctive combination of clinical features, including mild to severe intellectual disability, autism, severe speech and motor delay, and common facial characteristics. Brain abnormalities, behavioral problems, sleep disturbance, epilepsy, hypotonia, visual problems, congenital heart defects, gastrointestinal problems, short stature, and hormonal deficiencies are common comorbidities. Strikingly, individuals with the recurrent p.Tyr719* mutation were more severely affected.
CONCLUSIONS: This overview defines the full clinical spectrum of individuals with ADNP mutations, a specific autism subtype. We show that individuals with mutations in ADNP have many overlapping clinical features that are distinctive from those of other autism and/or intellectual disability syndromes. In addition, our data show preliminary evidence of a correlation between genotype and phenotype.
Copyright © 2018 Society of Biological Psychiatry. All rights reserved.

Entities:  

Keywords:  ADNP; Autism; Genetics; Helsmoortel-Van der Aa syndrome; Intellectual disability; Neurodevelopmental disorder

Mesh:

Substances:

Year:  2018        PMID: 29724491      PMCID: PMC6139063          DOI: 10.1016/j.biopsych.2018.02.1173

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  25 in total

1.  Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP gene.

Authors:  Małgorzata Krajewska-Walasek; Dorota Jurkiewicz; Dorota Piekutowska-Abramczuk; Marzena Kucharczyk; Krystyna H Chrzanowska; Aleksandra Jezela-Stanek; Elżbieta Ciara
Journal:  Am J Med Genet A       Date:  2016-03-31       Impact factor: 2.802

2.  Activity-dependent neuroprotective protein constitutes a novel element in the SWI/SNF chromatin remodeling complex.

Authors:  Shmuel Mandel; Illana Gozes
Journal:  J Biol Chem       Date:  2007-09-18       Impact factor: 5.157

3.  Activity-dependent neuroprotective protein: a novel gene essential for brain formation.

Authors:  Albert Pinhasov; Shmuel Mandel; Arkady Torchinsky; Eliezer Giladi; Zipora Pittel; Andrew M Goldsweig; Stephen J Servoss; Douglas E Brenneman; Illana Gozes
Journal:  Brain Res Dev Brain Res       Date:  2003-08-12

4.  Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease.

Authors:  Michael R Johnson; Kirill Shkura; Sarah R Langley; Andree Delahaye-Duriez; Prashant Srivastava; W David Hill; Owen J L Rackham; Gail Davies; Sarah E Harris; Aida Moreno-Moral; Maxime Rotival; Doug Speed; Slavé Petrovski; Anaïs Katz; Caroline Hayward; David J Porteous; Blair H Smith; Sandosh Padmanabhan; Lynne J Hocking; John M Starr; David C Liewald; Alessia Visconti; Mario Falchi; Leonardo Bottolo; Tiziana Rossetti; Bénédicte Danis; Manuela Mazzuferi; Patrik Foerch; Alexander Grote; Christoph Helmstaedter; Albert J Becker; Rafal M Kaminski; Ian J Deary; Enrico Petretto
Journal:  Nat Neurosci       Date:  2015-12-21       Impact factor: 24.884

Review 5.  A de novo convergence of autism genetics and molecular neuroscience.

Authors:  Niklas Krumm; Brian J O'Roak; Jay Shendure; Evan E Eichler
Journal:  Trends Neurosci       Date:  2013-12-30       Impact factor: 13.837

6.  HP1 recruits activity-dependent neuroprotective protein to H3K9me3 marked pericentromeric heterochromatin for silencing of major satellite repeats.

Authors:  Kerstin Mosch; Henriette Franz; Szabolcs Soeroes; Prim B Singh; Wolfgang Fischle
Journal:  PLoS One       Date:  2011-01-18       Impact factor: 3.240

7.  Synaptic, transcriptional and chromatin genes disrupted in autism.

Authors:  Silvia De Rubeis; Xin He; Arthur P Goldberg; Christopher S Poultney; Kaitlin Samocha; A Erucment Cicek; Yan Kou; Li Liu; Menachem Fromer; Susan Walker; Tarinder Singh; Lambertus Klei; Jack Kosmicki; Fu Shih-Chen; Branko Aleksic; Monica Biscaldi; Patrick F Bolton; Jessica M Brownfeld; Jinlu Cai; Nicholas G Campbell; Angel Carracedo; Maria H Chahrour; Andreas G Chiocchetti; Hilary Coon; Emily L Crawford; Sarah R Curran; Geraldine Dawson; Eftichia Duketis; Bridget A Fernandez; Louise Gallagher; Evan Geller; Stephen J Guter; R Sean Hill; Juliana Ionita-Laza; Patricia Jimenz Gonzalez; Helena Kilpinen; Sabine M Klauck; Alexander Kolevzon; Irene Lee; Irene Lei; Jing Lei; Terho Lehtimäki; Chiao-Feng Lin; Avi Ma'ayan; Christian R Marshall; Alison L McInnes; Benjamin Neale; Michael J Owen; Noriio Ozaki; Mara Parellada; Jeremy R Parr; Shaun Purcell; Kaija Puura; Deepthi Rajagopalan; Karola Rehnström; Abraham Reichenberg; Aniko Sabo; Michael Sachse; Stephan J Sanders; Chad Schafer; Martin Schulte-Rüther; David Skuse; Christine Stevens; Peter Szatmari; Kristiina Tammimies; Otto Valladares; Annette Voran; Wang Li-San; Lauren A Weiss; A Jeremy Willsey; Timothy W Yu; Ryan K C Yuen; Edwin H Cook; Christine M Freitag; Michael Gill; Christina M Hultman; Thomas Lehner; Aaarno Palotie; Gerard D Schellenberg; Pamela Sklar; Matthew W State; James S Sutcliffe; Christiopher A Walsh; Stephen W Scherer; Michael E Zwick; Jeffrey C Barett; David J Cutler; Kathryn Roeder; Bernie Devlin; Mark J Daly; Joseph D Buxbaum
Journal:  Nature       Date:  2014-10-29       Impact factor: 49.962

8.  Most genetic risk for autism resides with common variation.

Authors:  Trent Gaugler; Lambertus Klei; Stephan J Sanders; Corneliu A Bodea; Arthur P Goldberg; Ann B Lee; Milind Mahajan; Dina Manaa; Yudi Pawitan; Jennifer Reichert; Stephan Ripke; Sven Sandin; Pamela Sklar; Oscar Svantesson; Abraham Reichenberg; Christina M Hultman; Bernie Devlin; Kathryn Roeder; Joseph D Buxbaum
Journal:  Nat Genet       Date:  2014-07-20       Impact factor: 38.330

9.  Disruptive CHD8 mutations define a subtype of autism early in development.

Authors:  Raphael Bernier; Christelle Golzio; Bo Xiong; Holly A Stessman; Bradley P Coe; Osnat Penn; Kali Witherspoon; Jennifer Gerdts; Carl Baker; Anneke T Vulto-van Silfhout; Janneke H Schuurs-Hoeijmakers; Marco Fichera; Paolo Bosco; Serafino Buono; Antonino Alberti; Pinella Failla; Hilde Peeters; Jean Steyaert; Lisenka E L M Vissers; Ludmila Francescatto; Heather C Mefford; Jill A Rosenfeld; Trygve Bakken; Brian J O'Roak; Matthew Pawlus; Randall Moon; Jay Shendure; David G Amaral; Ed Lein; Julia Rankin; Corrado Romano; Bert B A de Vries; Nicholas Katsanis; Evan E Eichler
Journal:  Cell       Date:  2014-07-03       Impact factor: 41.582

10.  Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

Authors:  Holly A F Stessman; Bo Xiong; Bradley P Coe; Tianyun Wang; Kendra Hoekzema; Michaela Fenckova; Malin Kvarnung; Jennifer Gerdts; Sandy Trinh; Nele Cosemans; Laura Vives; Janice Lin; Tychele N Turner; Gijs Santen; Claudia Ruivenkamp; Marjolein Kriek; Arie van Haeringen; Emmelien Aten; Kathryn Friend; Jan Liebelt; Christopher Barnett; Eric Haan; Marie Shaw; Jozef Gecz; Britt-Marie Anderlid; Ann Nordgren; Anna Lindstrand; Charles Schwartz; R Frank Kooy; Geert Vandeweyer; Celine Helsmoortel; Corrado Romano; Antonino Alberti; Mirella Vinci; Emanuela Avola; Stefania Giusto; Eric Courchesne; Tiziano Pramparo; Karen Pierce; Srinivasa Nalabolu; David G Amaral; Ingrid E Scheffer; Martin B Delatycki; Paul J Lockhart; Fereydoun Hormozdiari; Benjamin Harich; Anna Castells-Nobau; Kun Xia; Hilde Peeters; Magnus Nordenskjöld; Annette Schenck; Raphael A Bernier; Evan E Eichler
Journal:  Nat Genet       Date:  2017-02-13       Impact factor: 38.330

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  38 in total

1.  Co-occurring medical conditions among individuals with ASD-associated disruptive mutations.

Authors:  Evangeline C Kurtz-Nelson; Jennifer S Beighley; Caitlin M Hudac; Jennifer Gerdts; Arianne S Wallace; Kendra Hoekzema; Evan E Eichler; Raphael A Bernier
Journal:  Child Health Care       Date:  2020-03-17

2.  From the Editors Desk: Angela Zawacki-Downing Writing to Professor Illana Gozes, Editor-in-Chief Journal of Molecular Neuroscience-Speaking from a Mother's Heart, AD's ADNP Syndrome.

Authors:  Angela Zawacki-Downing
Journal:  J Mol Neurosci       Date:  2019-08       Impact factor: 3.444

3.  Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation.

Authors:  Joseph Levine; David Cohen; Carole Herman; Alain Verloes; Vincent Guinchat; Lautaro Diaz; Cora Cravero; Anne Mandel; Illana Gozes
Journal:  J Mol Neurosci       Date:  2019-07       Impact factor: 3.444

4.  Mutations in ADNP affect expression and subcellular localization of the protein.

Authors:  Elisa Cappuyns; Jolien Huyghebaert; Geert Vandeweyer; R Frank Kooy
Journal:  Cell Cycle       Date:  2018-07-17       Impact factor: 4.534

5.  ADNP differentially interact with genes/proteins in correlation with aging: a novel marker for muscle aging.

Authors:  Oxana Kapitansky; Illana Gozes
Journal:  Geroscience       Date:  2019-07-01       Impact factor: 7.713

6.  Developmental Predictors of Cognitive and Adaptive Outcomes in Genetic Subtypes of Autism Spectrum Disorder.

Authors:  Anne B Arnett; Jennifer S Beighley; Evangeline C Kurtz-Nelson; Kendra Hoekzema; Tianyun Wang; Raphe A Bernier; Evan E Eichler
Journal:  Autism Res       Date:  2020-09-12       Impact factor: 5.216

7.  Activity-dependent neuroprotective protein deficiency models synaptic and developmental phenotypes of autism-like syndrome.

Authors:  Gal Hacohen-Kleiman; Shlomo Sragovich; Gidon Karmon; Andy Y L Gao; Iris Grigg; Metsada Pasmanik-Chor; Albert Le; Vlasta Korenková; R Anne McKinney; Illana Gozes
Journal:  J Clin Invest       Date:  2018-09-24       Impact factor: 14.808

8.  The autism spectrum phenotype in ADNP syndrome.

Authors:  Anne B Arnett; Candace L Rhoads; Kendra Hoekzema; Tychele N Turner; Jennifer Gerdts; Arianne S Wallace; Sandra Bedrosian-Sermone; Evan E Eichler; Raphael A Bernier
Journal:  Autism Res       Date:  2018-08-14       Impact factor: 5.216

9.  Sex-and Region-Dependent Expression of the Autism-Linked ADNP Correlates with Social- and Speech-Related Genes in the Canary Brain.

Authors:  Gal Hacohen-Kleiman; Stan Moaraf; Oxana Kapitansky; Illana Gozes
Journal:  J Mol Neurosci       Date:  2020-09-14       Impact factor: 3.444

10.  Activity-dependent neuroprotective protein (ADNP) is an alcohol-responsive gene and negative regulator of alcohol consumption in female mice.

Authors:  Illana Gozes; Segev Barak; Yarden Ziv; Nofar Rahamim; Noa Lezmy; Oren Even-Chen; Ohad Shaham; Anna Malishkevich; Eliezer Giladi; Ran Elkon
Journal:  Neuropsychopharmacology       Date:  2018-06-27       Impact factor: 7.853

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