Evidence map›Paper›PMID 42825826›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Clinical spectrum and genetic landscape of MTHFR deficiency: a cohort study including novel variants.

Ozge Kamer Karalar Pekuz, Pelin Teke Kisa, Sevil Yildiz, Mehmet Kocabey, Tanyel Zubarioglu, Zumrut Arslan Gulten, Emine Sedef Sezen, Esra Er, Serdar Pekuz, Banu Kadioglu Yilmaz and 11 more

Abstract readMulticenter Study
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In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Ozge Kamer Karalar PekuzDepartment of Inherited Metabolic Disorders, Dokuz Eylül University, Izmir, Türkiye.ORCID http://orcid.org/0000-0002-1048-4139
Pelin Teke KisaDepartment of Inherited Metabolic Disorders, Dokuz Eylül University, Izmir, Türkiye. pelin.tekekisa@gmail.com.ORCID http://orcid.org/0000-0001-6481-3172
Sevil YildizDepartment of Inherited Metabolic Disorders, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Türkiye.ORCID http://orcid.org/0000-0001-6947-2573
Mehmet KocabeyDepartment of Medical Genetics, Dokuz Eylül University, İzmir, Türkiye.ORCID http://orcid.org/0000-0001-9565-6907
Tanyel ZubariogluDepartment of Pediatric Nutrition and Metabolism, Cerrahpaşa Medical Faculty, İstanbul University-Cerrahpasa, İstanbul, Türkiye.ORCID http://orcid.org/0000-0002-7159-4008
Zumrut Arslan GultenDepartment of Inherited Metabolic Disorders, Sisli Hamidiye Etfal Training and Research Hospital, Istanbul, Türkiye.ORCID http://orcid.org/0000-0003-4970-1759
Emine Sedef SezenDepartment of Inherited Metabolic Disorders, Bursa Uludag University, Bursa, Türkiye.ORCID http://orcid.org/0009-0007-4707-3847
Esra ErDepartment of Inherited Metabolic Disorders, Dr. Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Türkiye.ORCID http://orcid.org/0000-0001-8867-0508
Serdar PekuzDepartment of Pediatric Neurology, Çukurova University, Adana, Türkiye.ORCID http://orcid.org/0000-0002-1686-7536
Banu Kadioglu YilmazDepartment of Inherited Metabolic Disorders, Selcuk University, Konya, Türkiye.ORCID http://orcid.org/0000-0002-5521-7659
Melis KirmizitasDepartment of Inherited Metabolic Disorders, Dokuz Eylül University, Izmir, Türkiye.ORCID http://orcid.org/0009-0009-4062-4364
Meral Bahar IsterDepartment of Inherited Metabolic Disorders, Kocaeli University, Kocaeli, Türkiye.ORCID http://orcid.org/0000-0002-3315-6664
Bahar KuluDepartment of Inherited Metabolic Disorders, Dokuz Eylül University, Izmir, Türkiye.ORCID http://orcid.org/0000-0003-2147-9316
Filiz HazanDepartment of Medical Genetics, Dr. Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Türkiye.ORCID http://orcid.org/0000-0002-0382-3446
Mustafa KilicDepartment of Pediatrics, Metabolism Unit, Ankara Etlik City Hospital, University Of Health Sciences, Ankara, Türkiye.ORCID http://orcid.org/0000-0002-1401-5233
Ozlem Unal UzunDepartment of Inherited Metabolic Disorders, Kocaeli University, Kocaeli, Türkiye.ORCID http://orcid.org/0000-0001-7937-7721
Ertugrul KiykimDepartment of Pediatric Nutrition and Metabolism, Cerrahpaşa Medical Faculty, İstanbul University-Cerrahpasa, İstanbul, Türkiye.ORCID http://orcid.org/0000-0001-5170-5594
Halil Ibrahim AydinDepartment of Inherited Metabolic Disorders, Baskent University , Ankara, Türkiye.ORCID http://orcid.org/0000-0001-7994-4394
Sahin ErdolDepartment of Inherited Metabolic Disorders, Bursa Uludag University, Bursa, Türkiye.ORCID http://orcid.org/0000-0003-4402-9609
Ayse Cigdem Aktuglu ZeybekDepartment of Pediatric Nutrition and Metabolism, Cerrahpaşa Medical Faculty, İstanbul University-Cerrahpasa, İstanbul, Türkiye.ORCID http://orcid.org/0000-0001-7256-0750
Nur ArslanDepartment of Inherited Metabolic Disorders, Dokuz Eylül University, Izmir, Türkiye.ORCID http://orcid.org/0000-0003-3151-3741

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methylene tetrahydrofolate reductase (MTHFR) deficiency is a rare inherited metabolic disorder that impairs myelination and brain development, leading to primary clinical manifestations, particularly neurological deficits. The aim of this study was to comprehensively describe the clinical presentation, biochemical profile, and molecular spectrum of patients with MTHFR deficiency. This multicenter, retrospective, descriptive study evaluated the medical records of 19 patients diagnosed with MTHFR deficiency at ten metabolic disease centers. A total of 13 patients had early-onset disease. In the early-onset group, all patients had varying degrees of neurodevelopmental delay. The median diagnostic delay from the first symptom to diagnosis was 3 months in early-onset cases and 118 months in late-onset cases. MTHFR deficiency exhibits a broad clinical spectrum, with acute deterioration possible even in chronically affected patients. MTHFR deficiency should be considered among treatable neurometabolic disorders in patients with otherwise unexplained neurodevelopmental or neuropsychiatric manifestations, particularly when accompanied by additional neurological findings.

Indexed as

Developmental DisabilitiesHomocystinuriaMethylenetetrahydrofolate Reductase (NADPH2)Muscle SpasticityPsychotic DisordersAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanDevelopmental delayEpilepsyFolateHomocysteineMethylene tetrahydrofolate reductase deficiencyMTHFRMTHFR deficiency

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Registered trials

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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.