Evidence map›Paper›PMID 42204984›Full record

ArticleClinical genetics2026

GAA-FGF14 Ataxia Is a Frequently Overlooked Cause of Sporadic Adult-Onset Ataxia.

Eva-Maria Kraus, Johannes Lenz, Pauline Ploettner, Patricia Duffek, Jost-Julian Rumpf, Rami Abou Jamra, John Wiedenhoeft, Denny Popp

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Article in Clinical 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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1 · What the graph read from it

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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

8 authors.

Eva-Maria KrausInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.ORCID https://orcid.org/0000-0002-6152-8971
Johannes LenzInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Pauline PloettnerDepartment of Neurology, University of Leipzig Medical Center, Leipzig, Germany.
Patricia DuffekInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Jost-Julian RumpfDepartment of Neurology, University of Leipzig Medical Center, Leipzig, Germany.ORCID https://orcid.org/0000-0002-7357-713X
Rami Abou JamraInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
John WiedenhoeftInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Denny PoppInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GAA-FGF14 ataxia (spinocerebellar ataxia 27B, SCA27B), identified in 2023, is a major cause of adult-onset autosomal dominant cerebellar ataxia (ADCA). In this study, we assessed the frequency of GAA-FGF14 ataxia in a predominantly sporadic German cohort of 107 genetically unresolved index patients using long-range PCR and nanopore sequencing. Somatic mosaicism of GAA repeat length was assessed using a custom bioinformatics pipeline based on a modified cyclic Smith-Waterman algorithm. This approach provided streamlined detection and enabled precise genotyping. Among sporadic cases, 10% had a pathogenic and 6% an intermediate repeat expansion. Across the entire cohort, 13% carried a pathogenic and 5% an intermediate repeat expansion. Diagnostic yield varied substantially by clinical presentation: 50% in cases with typical GAA-FGF14-ataxia features, 13% in patients with compatible but less characteristic features and 5% in atypical presentations. In conclusion, this study further corroborates existing evidence that GAA-FGF14 ataxia is a frequent cause of both sporadic and familial cerebellar ataxia. Given its high diagnostic yield and the limited detectability by standard short-read genome sequencing, targeted testing should be more widely implemented.

Indexed as

Cerebellar AtaxiaFibroblast Growth FactorsGenetic Predisposition to DiseaseSpinocerebellar AtaxiasSpinocerebellar DegenerationsAdultAgedAge of OnsetFemaleGenotypeHumansMaleMiddle AgedMosaicismNanopore SequencingTrinucleotide Repeat Expansionfibroblast growth factor 14Fibroblast Growth FactorsataxiaGAA‐FGF14‐ataxiananopore sequencingrepeat expansion disordersSCA27Bspinocerebellar ataxia 27B

Identifiers

PMID42204984
PMCPMC13432038

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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.