{"entity": "researcher", "timestamp": "2026-08-18T02:06:21.173Z", "family": "Sperker", "given": "Wolfgang", "initials": "W", "orcid": "0000-0002-5351-9418", "affiliations": ["From the Departments of Neurology (I.B.-S.) and Internal Medicine (W.S.), Sunderby Hospital, Lule\u00e5; Ume\u00e5 University (I.B.-S.); Department of Clinical Genetics (M.K.), Centre for Inherited Metabolic Diseases (H.B., A.W., R.W., M.E.), Karolinska University Hospital, Stockholm; Departments of Medical Biochemistry and Biophysics (A.W.), Oncology and Pathology (I.N.), Molecular Medicine and Surgery (M.E.), and Neurology (M.P.), Karolinska Institutet, Stockholm, Sweden."], "links": {"self": {"href": "https://publications.scilifelab.se/researcher/f4aa72d100f6463e9b3327bab3fbd239.json"}, "display": {"href": "https://publications.scilifelab.se/researcher/f4aa72d100f6463e9b3327bab3fbd239"}}, "publications": [{"entity": "publication", "iuid": "ad68a32317274c03aa068006b44d02b9", "links": {"self": {"href": "https://publications.scilifelab.se/publication/ad68a32317274c03aa068006b44d02b9.json"}, "display": {"href": "https://publications.scilifelab.se/publication/ad68a32317274c03aa068006b44d02b9"}}, "title": "Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.", "authors": [{"family": "Ben-Shabat", "given": "Ilan", "initials": "I", "orcid": "0000-0003-2211-7528", "researcher": {"href": "https://publications.scilifelab.se/researcher/f19650307eff4a4691585bdef569c414.json"}}, {"family": "Kvarnung", "given": "Malin", "initials": "M", "orcid": "0000-0003-0193-0165", "researcher": {"href": "https://publications.scilifelab.se/researcher/77c2ad2b3e1442f5937aded8e129994a.json"}}, {"family": "Sperker", "given": "Wolfgang", "initials": "W", "orcid": "0000-0002-5351-9418", "researcher": {"href": "https://publications.scilifelab.se/researcher/f4aa72d100f6463e9b3327bab3fbd239.json"}}, {"family": "Bruhn", "given": "Helene", "initials": "H"}, {"family": "Wredenberg", "given": "Anna", "initials": "A", "orcid": "0000-0002-2500-6121", "researcher": {"href": "https://publications.scilifelab.se/researcher/3ea9ee7305424cdb8c238ef569e5be03.json"}}, {"family": "Wibom", "given": "Rolf", "initials": "R", "orcid": "0000-0001-6721-4642", "researcher": {"href": "https://publications.scilifelab.se/researcher/c7d5fc666ef84a8784d8b28ecf233146.json"}}, {"family": "Nennesmo", "given": "Inger", "initials": "I", "orcid": "0009-0000-0871-1147", "researcher": {"href": "https://publications.scilifelab.se/researcher/7422a07a064648a5a1dfed8a9889503b.json"}}, {"family": "Engvall", "given": "Martin", "initials": "M"}, {"family": "Paucar", "given": "Martin", "initials": "M", "orcid": "0000-0003-3735-1480", "researcher": {"href": "https://publications.scilifelab.se/researcher/bbc592904eb5402ea48a624471d4b939.json"}}], "type": "journal article", "published": "2023-12-00", "journal": {"title": "Neurol Genet", "issn": "2376-7839", "volume": "9", "issue": "6", "pages": "e200100", "issn-l": "2376-7839"}, "abstract": "Biallelic variants in XPNPEP3 are associated with a rare mitochondrial syndrome characterized by nephronophthisis leading to kidney failure, essential tremor, hearing loss, seizures, and intellectual disability. Only 2 publications on this condition are available. We report a man with a complex ataxia syndrome, hearing loss, and kidney failure associated with a new biallelic variant in XPNPEP3.\n\nClinical evaluation, neuroimaging studies, a kidney biopsy, and whole genome sequencing (WGS) were applied. Since the phenotype was compatible with a mitochondrial disease, a muscle biopsy with morphological and mitochondrial biochemical investigations was performed.\n\nAxial ataxia, cerebellar atrophy, hearing loss, myopathy, ptosis, supranuclear palsy, and kidney failure because of nephronophthisis were the prominent features in this case. WGS revealed the novel biallelic variant c.766C>T (p.Gln256*) in XPNPEP3. A muscle biopsy revealed COX negative fibers, a few ragged red fibers, and ultrastructural mitochondrial changes. Enzyme activity in respiratory chain complex IV was reduced in muscle and fibroblasts.\n\nThis is the first report of a slowly progressive cerebellar ataxia associated with a novel biallelic variant in XPNPEP3. Abnormalities typical for mitochondrial disease and the slow progression of kidney disease are also striking. Our report expands the spectrum of XPNPEP3-related diseases.", "doi": "10.1212/NXG.0000000000200100", "pmid": "38035175", "labels": {"Clinical Genomics Stockholm": "Service", "Clinical Genomics": "Service"}, "xrefs": [{"db": "pmc", "key": "PMC10684053"}, {"db": "pii", "key": "NXG-2023-000165"}], "notes": [], "created": "2024-11-21T10:09:19.210Z", "modified": "2024-11-21T10:28:20.978Z"}]}