Evidence map›Paper›PMID 41450729›Full record

ArticleNeurology. Genetics2026

DNAJC12 Disease: Clinical Spectrum and Long-Term Outcomes.

Filippo Manti, Giacomina Ricciardi, Francesca Nardecchia, Manuela Tolve, Cristiana Artiola, Maria Teresa Carbone, Claudia Carducci, Davide Mei, Francesco Porta, Rita Ortolano and 6 more

Abstract read
In one paragraph

Article in Neurology. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Molecular genetics and metabolism reports · 2026
    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

16 authors.

Filippo MantiDepartment of Human Neuroscience, Unit of Child Neurology and Psychiatry, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0002-2012-8410
Giacomina RicciardiDepartment of Human Neuroscience, Unit of Child Neurology and Psychiatry, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0003-0686-2499
Francesca NardecchiaDepartment of Human Neuroscience, Unit of Child Neurology and Psychiatry, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0002-0808-2827
Manuela TolveClinical Pathology Unit, AOU Policlinico Umberto I, Rome, Italy.ORCID https://orcid.org/0000-0003-0263-4325
Cristiana ArtiolaClinical Pathology Unit, AOU Policlinico Umberto I, Rome, Italy.ORCID https://orcid.org/0009-0002-7717-6752
Maria Teresa CarboneUOS Metabolic and Rare Diseases, Santobono Hospital, Napoli, Italy.ORCID https://orcid.org/0000-0003-0205-9711
Claudia CarducciDepartment of Experimental Medicine, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0003-0515-9208
Davide MeiNeuroscience and Medical Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-6790-6251
Francesco PortaDepartment of Pediatrics, AOU Città della Salute e della Scienza di Torino, University of Torino, Turin, Italy.ORCID https://orcid.org/0000-0003-3899-4867
Rita OrtolanoDepartment of Medical and Surgical Sciences, Pediatric Unit, Regional Centre for Expanded Newborn Screening, S. Orsola-Malpighi University Hospital, Bologna, Italy; and.ORCID https://orcid.org/0000-0001-8218-1463
Egidio CandelaDepartment of Medical and Surgical Sciences, Pediatric Unit, Regional Centre for Expanded Newborn Screening, S. Orsola-Malpighi University Hospital, Bologna, Italy; and.ORCID https://orcid.org/0000-0002-4573-9314
Alberto BurlinaDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health, Reference Centre Expanded Newborn Screening, University Hospital, Padua, Italy.ORCID https://orcid.org/0000-0001-7724-137X
Renzo GuerriniNeuroscience and Medical Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0002-7272-7079
Francesco PisaniDepartment of Human Neuroscience, Unit of Child Neurology and Psychiatry, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0002-1083-5576
Antonio AngeloniDepartment of Experimental Medicine, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0003-4969-9548
Vincenzo LeuzziDepartment of Human Neuroscience, Unit of Child Neurology and Psychiatry, Sapienza University of Rome, Italy.ORCID https://orcid.org/0000-0002-2314-6139

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Autosomal recessive DNAJC12 disease, the most recently identified disorder of biogenic amine synthesis, presents with a broad clinical spectrum and variable outcomes, ranging from asymptomatic patients to early-onset parkinsonism. This study aimed to better outline the clinical phenotype and outcomes of DNAJC12 disease, the prognostic value of the metabolic and genetic biomarkers, and the treatment response. Methods: We systematically collected clinical, biochemical, and genetic data from 56 patients with DNAJC12 disease in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines: 51 from the literature since the disease was first described and 5 unpublished personal cases. Results: Three prevalent clinical patterns of presentation and outcome were identified: (1) asymptomatic condition, (2) neurodevelopmental disorders (NDD) leading to intellectual disability with psychiatric issues and dystonia-parkinsonism (D-P) during the second decade of life in some patients, and (3) early-onset static l-dopa-responsive parkinsonism in previously asymptomatic adult patients. Hyperphenylalaninemia was the most consistent metabolic alteration. CSF depletion of homovanillic acid (HVA) and 5-HIAA was detected in 18 and 20 of 29 symptomatic patients, respectively. Three stepwise regression analyses identified significant predictors of clinical outcomes in patients with phenylketonuria (PKU). CSF HVA levels and phenylalanine levels at diagnosis predicted the occurrence of D-P, while 26% of intellectual disability variability was explained by CSF HVA at diagnosis, and 31% of psychiatric disorder variability by later age at diagnosis. The phenotype was consistently associated with only a few Discussion: DNAJC12 disease is a new metabolic neurodevelopmental disorder linked to parkinsonism. The combined effects of neurotransmitter depletion and disrupted enzyme proteostasis in dopaminergic and serotoninergic neurons may underlie the early neurodevelopmental presentation and subsequent neurologic and psychiatric disorders.

Identifiers

PMID41450729
PMCPMC12737867

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