Evidence map›Paper›PMID 41734767›Full record

ArticleAmerican journal of human genetics2026

Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities.

Davut Pehlivan, Abigail Sandoval, Reza Maroofian, François Lecoquierre, Aisha M Al Shamsi, Gyu S Lee, Osman Yesilbas, Preston Taylor, Matthew B McDougal, Vahid Bahrambeigi and 26 more

Abstract read
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Article in American journal of human genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

36 authors.

Davut PehlivanSection of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Texas Children's Hospital, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
Abigail SandovalAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Reza MaroofianCentre for Neuromuscular Diseases, Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, WC1N 3BG London, UK.
François LecoquierreDepartment of Genetics and Reference Center for Developmental Disorders, University Rouen Normandie, Inserm U1245 and CHU Rouen, 76000 Rouen, France.
Aisha M Al ShamsiDepartment of Pediatrics, Division of Genetic and Metabolic, Tawam Hospital, Al Ain, United Arab Emirates.
Gyu S LeeAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Osman YesilbasDivision of Pediatric Critical Care Medicine, Ataşehir Memorial Hospital, İstanbul, Türkiye.
Preston TaylorAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Matthew B McDougalAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Vahid BahrambeigiDiagnostic Genetics and Genomics, Yale University School of Medicine, New Haven, CT, USA.
Omid AryaniNeuroscience Department, Iran University of Medical Sciences, Tehran, Iran.
Juan Felipe RamirezAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Khalid Hama SalihClinical Science, College of Medicine, University of Sulaimani, Sulaymaniyah, Iraq.
Chadi Al AlamDivision of Pediatric Neurology, American Center for Psychiatry and Neurology, Abu Dhabi and Al Ain, United Arab Emirates.
Heba MorsyCentre for Neuromuscular Diseases, Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, WC1N 3BG London, UK; Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Haytham HussienKuwait Hospital, Block1, Sabah Al-Salem, Kuwait.
Tarek OmarNeurology Unit, Department of Pediatrics, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Ibrahim M AbdelrazekDepartment of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Anne Claire BrehinDepartment of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, U1245 and Rouen University Hospital, Inserm, 76000 Rouen, France.
Dana MarafiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Tugba KalayciDepartment of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Jubran Abu RahmaNeuropediatric, Clalit Health Services, Haifa and West Galilee, Israel.
Jawabreh Kassem TalbeyaDepartment of Radiology, The Bnai Zion Medical Center, Haifa, Israel.
Husein DabbahPediatrics, Clalit Health Services, Haifa and West Galilee, Israel.
Eric VerspyckDepartment of Obstetrics and Gynecology, Rouen University Hospital, Rouen, France.
Toktam MoosavianPediatric Department, Pediatric Neurology Department, Loghman Hakim Hospital, Shanid Beheshti University of Medical Sciences, Tehran, Iran.
Jawid M FatihDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Tadahiro MitaniDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Gulsen AkayDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Daniel G CalameDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Anne-Marie GuerrotDepartment of Genetics and Reference Center for Developmental Disorders, University Rouen Normandie, Inserm U1245 and CHU Rouen, 76000 Rouen, France.
Wendy K ChungDepartment of Pediatrics, Boston Children's Hospital and Harvard Medical School, Brookline, MA, USA.
Henry HouldenCentre for Neuromuscular Diseases, Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, WC1N 3BG London, UK.
James R LupskiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Texas Children's Hospital, Houston, TX, USA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Adel ShalataThe Simon Winter Institute for Human Genetics, Bnai Zion Medical Center, The Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa 32000, Israel. Electronic address: adel.shalata@b-zion.org.il.
Wan Hee YoonAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA. Electronic address: wanhee-yoon@omrf.org.

Funding

Frequency of variants of unknown significance by ancestry groups in the All of Us Research Program cohortU01HG011758 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI RICHARD A GIBBS, JAMES R. LUPSKI · 2021 to 2026
$13.8M
STRUCTURAL VARIATION IN NEUROLOGICAL DISEASER35NS105078 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI LUPSKI, JAMES R. · 2018 to 2025
$6.0M
GEROSCIENCE TRAINING PROGRAM IN OKLAHOMAT32AG052363 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Benjamin Francis Miller, William Edmund Sonntag · 2017 to 2026
$3.6M
Role of ATAD3A in Lysosomal Homeostasis and NeurogenesisR01NS121298 · NINDS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI YOON, WAN HEE · 2021 to 2025
$2.2M
NHGRI NIH HHS U01 HG011758NIA NIH HHS T32 AG052363NINDS NIH HHS R01 NS121298NINDS NIH HHS R35 NS105078
6 · The paper itself

Abstract

Nardilysin (NRDC) plays a role in multiple cellular functions in diverse cellular compartments, including ectodomain shedding in the plasma membrane, as well as chaperoning a key Krebs cycle enzyme in mitochondria. We had previously reported limited clinical information from two individuals with homozygous frameshift variants in NRDC. With inclusion of previously published individuals, here we report 14 individuals (10 females, four males) from nine unrelated families carrying homozygous NRDC pathogenic variants. Common clinical features include severe to profound developmental delay/intellectual disability (12/12), microcephaly (13/13), prematurity (5/13), lethality in the first 3 years of life (9/14), seizures (7/11), joint contractures (4/8), eye/visual abnormalities (5/7), and abnormal brain imaging studies ranging from diffuse atrophy to lissencephaly (8/11). The identified variants include two splice, three frameshift, and three missense variants. RT-PCR from affected individual fibroblasts and a minigene assay in HEK293T cells demonstrate that the splice variants led to exon skipping of NRDC. To further investigate the pathogenicity of the variants in vivo, we used the Drosophila Nrdc (dNrdc) mutant model. dNrdc null mutants caused developmental lethality, which is fully rescued by wild-type human NRDC. Studies in the Drosophila dNrdc mutant models showed that both splice variants and frameshift variants cause severe loss of function, leading to lethality, whereas missense variants cause partial lethality and short lifespan, consistent with less severe phenotype. Our data establish that homozygous variants in NRDC are pathogenic, leading to highly lethal and severe neurodevelopmental disorder in humans.

Indexed as

BrainMetalloendopeptidasesMicrocephalyNeurodevelopmental DisordersAllelesAnimalsChildChild, PreschoolCytokinesFemaleFrameshift MutationHEK293 CellsHomozygoteHumansInfantInfant, NewbornCytokinesMetalloendopeptidasesNeoplasm ProteinsRNA-Binding Proteinssmall inducible cytokine subfamily E, member 1lethalitymicrocephalymitochondrianeurodevelopmental disorderNRD1NRDC

Identifiers

PMID41734767
PMCPMC13087469

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