Evidence map›Paper›PMID 32761064›Full record

ArticleBrain : a journal of neurology2020

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.

Pauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy, Daniela Buhas, Stephanie Fox, Jane Juusola, Majid Alfadhel and 36 more

Registry-linked trialOpen access · bronzeAbstract readCase Reports
In one paragraph

Article in Brain : a journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02450851 (Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02450851 recruitingnot on this map

Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network

TypeobservationalSponsorNational Human Genome Research Institute (NHGRI)Ran2015 to 2028Enrolled20,000ConditionsGenetic Disease
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Genetic Profiling of Polymicrogyria in a South Indian Cohort.Annals of Indian Academy of Neurology · 2025
    Article
  7. Biallelic variants in the conserved ribosomal protein chaperone geneProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
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  10. Article
  11. Article
  12. Article
  13. Article
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  15. Article
  16. Article
  17. Article
  18. Genetic pain loss disorders.Nature reviews. Disease primers · 2022
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

46 authors at 20 institutions in 10 countries.

Pauline E SchneebergerInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Fanny KortümInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Georg Christoph KorenkeKlinik für Neuropädiatrie und angeborene Stoffwechselerkrankungen, Klinikum Oldenburg, Oldenburg, Germany.
Malik AlawiBioinformatics Core Unit, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
René SanterDepartment of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mathias WoidyDepartment of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Daniela BuhasDivision of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, Canada.
Stephanie FoxDivision of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, Canada.
Jane JuusolaGeneDx, Gaithersburg, USA.
Majid AlfadhelDivision of Genetics, Department of Pediatrics, King Abdullah specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs (MNGHA), Riyadh, Saudi Arabia.
Bryn D WebbDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA.
Emanuele G CociDepartment for Neuropediatrics, University Children's Hospital, Ruhr University Bochum, Bochum, Germany.
Rami Abou JamraInstitute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
Manuela SiekmeyerUniversitätsklinikum Leipzig - AöR, University of Leipzig, Hospital for Children and Adolescents, Leipzig, Germany.
Saskia BiskupCeGaT GmbH and Praxis für Humangenetik Tübingen, Tübingen, Germany.
Corina HellerCeGaT GmbH and Praxis für Humangenetik Tübingen, Tübingen, Germany.
Esther M MaierDr. von Hauner Children's Hospital, University of Munich, Munich, Germany.
Poupak Javaher-HaghighiMedicover Humangenetik Hannover, Hanover, Germany.
Maria F BedeschiMedical Genetic Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Paola F AjmoneChild and Adolescent Neuropsychiatric Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.
Maria IasconeLaboratorio di Genetica Medica, ASST Papa Giovanni XXIII, Bergamo, Italy.
Hilde PeetersCenter for Human Genetics, KU Leuven, Leuven, Belgium.
Katleen BallonCentre for Developmental Disabilities, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Jaak JaekenCenter for Metabolic Diseases, KU Leuven, Leuven, Belgium.
Aroa Rodríguez AlonsoUnidad de Patología Compleja, Servicio de Pediatría, Hospital Universitario La Paz, Madrid, Spain.
María Palomares-BraloInstituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
Fernando Santos-SimarroInstituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
Marije E C MeuwissenCenter of Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.
Diane BeysenDepartment of Pediatric Neurology, University Hospital Antwerp, Antwerp, Belgium.
R Frank KooyDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Henry HouldenDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
David MurphyDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
Mohammad DoostiNext Generation Genetic Polyclinic, Mashhad, Iran.
Ehsan G KarimianiNext Generation Genetic Polyclinic, Mashhad, Iran.
Majid MojarradDepartment of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Reza MaroofianDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
Lenka NoskovaResearch Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Stanislav KmochResearch Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Tomas HonzikDepartment of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Heidi CopeDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
Amarilis Sanchez-ValleDivision of Genetics and Metabolism, College of Medicine, University of South Florida, Tampa, Florida, USA.
Undiagnosed Diseases Network
Bruce D GelbDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA.
Ingo KurthInstitute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Maja HempelInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Kerstin KutscheInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Universität Hamburg · DEMcGill University Health Centre · CANational Hospital for Neurology and Neurosurgery · GBKU Leuven · BECharles University · CZAntwerp University Hospital · BEChild Health and Development Institute · USDuke Medical Center · USHospital Universitario La Paz · ESMedicover · DEFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITKlinikum Oldenburg · DEPraxis für Humangenetik Tübingen · DEKing Saud bin Abdulaziz University for Health Sciences · SALeipzig University · DELudwig-Maximilians-Universität München · DEMashhad University of Medical Sciences · IROspedale Papa Giovanni XXIII · ITSt George's, University of London · GBUniversity Hospital Leipzig · DE

Funding

An integrated and diverse genomic medicine program for undiagnosed diseasesU01HG007672 · NHGRI · DUKE UNIVERSITY · PI SHASHI, VANDANA · 2014 to 2022
$13.4M
Clinical Sequencing Core Facility for the Undiagnosed Diseases Network (UDN)U01HG007942 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI ENG, CHRISTINE · 2014 to 2021
$10.2M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
Transforming Genomics with 5 PB Big Omics Data Engine Cray CS300-AC SupercomputerS10OD018522 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2014 to 2014
$1.9M
NHGRI NIH HHS U01 HG007672NHGRI NIH HHS U01 HG007942NIH HHS S10 OD018522NIH HHS S10 OD026880
6 · The paper itself

Abstract

In pleiotropic diseases, multiple organ systems are affected causing a variety of clinical manifestations. Here, we report a pleiotropic disorder with a unique constellation of neurological, endocrine, exocrine, and haematological findings that is caused by biallelic MADD variants. MADD, the mitogen-activated protein kinase (MAPK) activating death domain protein, regulates various cellular functions, such as vesicle trafficking, activity of the Rab3 and Rab27 small GTPases, tumour necrosis factor-α (TNF-α)-induced signalling and prevention of cell death. Through national collaboration and GeneMatcher, we collected 23 patients with 21 different pathogenic MADD variants identified by next-generation sequencing. We clinically evaluated the series of patients and categorized the phenotypes in two groups. Group 1 consists of 14 patients with severe developmental delay, endo- and exocrine dysfunction, impairment of the sensory and autonomic nervous system, and haematological anomalies. The clinical course during the first years of life can be potentially fatal. The nine patients in Group 2 have a predominant neurological phenotype comprising mild-to-severe developmental delay, hypotonia, speech impairment, and seizures. Analysis of mRNA revealed multiple aberrant MADD transcripts in two patient-derived fibroblast cell lines. Relative quantification of MADD mRNA and protein in fibroblasts of five affected individuals showed a drastic reduction or loss of MADD. We conducted functional tests to determine the impact of the variants on different pathways. Treatment of patient-derived fibroblasts with TNF-α resulted in reduced phosphorylation of the extracellular signal-regulated kinases 1 and 2, enhanced activation of the pro-apoptotic enzymes caspase-3 and -7 and increased apoptosis compared to control cells. We analysed internalization of epidermal growth factor in patient cells and identified a defect in endocytosis of epidermal growth factor. We conclude that MADD deficiency underlies multiple cellular defects that can be attributed to alterations of TNF-α-dependent signalling pathways and defects in vesicular trafficking. Our data highlight the multifaceted role of MADD as a signalling molecule in different organs and reveal its physiological role in regulating the function of the sensory and autonomic nervous system and endo- and exocrine glands.

Indexed as

Death Domain Receptor Signaling Adaptor ProteinsDevelopmental DisabilitiesGuanine Nucleotide Exchange FactorsHumansMutationNervous System DiseasesPhenotypeProtein TransportSignal TransductionDeath Domain Receptor Signaling Adaptor ProteinsGuanine Nucleotide Exchange FactorsMADD protein, humanDENNHSANintellectual disabilitymultisystemwhole-exome sequencing

Identifiers

PMID32761064
PMCPMC7447524
OpenAlexW3048226301

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.