Evidence map›Paper›PMID 37373807›Full record

ArticleJournal of clinical medicine2023

CNS Manifestations in Mucolipidosis Type II-A Retrospective Analysis of Longitudinal Data on Neurocognitive Development and Neuroimaging in Eleven Patients.

Luise Sophie Ammer, Karolin Täuber, Anna Perez, Thorsten Dohrmann, Jonas Denecke, René Santer, Ulrike Blümlein, Ann-Kathrin Ozga, Sandra Pohl, Nicole Maria Muschol

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Novel Phenotypical and Biochemical Findings in Mucolipidosis Type II.International journal of molecular sciences · 2025
    Article
  4. Article
  5. 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

10 authors at 2 institutions in 1 country.

Luise Sophie AmmerInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Karolin TäuberInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Anna PerezInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Thorsten DohrmannDepartment of Anaesthesiology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-3737-2778
Jonas DeneckeInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
René SanterInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-3670-5657
Ulrike BlümleinDepartment of Paediatrics, Carl-Thiem-Klinikum gGmbH, 03048 Cottbus, Germany.
Ann-Kathrin OzgaInstitute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Sandra PohlInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-7409-7042
Nicole Maria MuscholInternational Centre for Lysosomal Disorders (ICLD), Department of Paediatrics, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Universität Hamburg · DECarl-Thiem-Klinikum Cottbus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucolipidosis type II (MLII), an ultra-rare lysosomal storage disorder, manifests as a fatal multi-systemic disease. Mental inhibition and progressive neurodegeneration are commonly reported disease manifestations. Nevertheless, longitudinal data on neurocognitive testing and neuroimaging lack in current literature. This study aimed to provide details on central nervous system manifestations in MLII. All MLII patients with at least one standardized developmental assessment performed between 2005 and 2022 were included by retrospective chart review. A multiple mixed linear regression model was applied. Eleven patients with a median age of 34.0 months (range 1.6-159.6) underwent 32 neurocognitive and 28 adaptive behaviour assessments as well as 14 brain magnetic resonance imagings. The scales used were mainly BSID-III (42%) and VABS-II (47%). Neurocognitive testing (per patient: mean 2.9, standard deviation (SD) 2.0) performed over 0-52.1 months (median 12.1) revealed profound impairment with a mean developmental quotient of 36.7% (SD 20.4) at last assessment. The patients showed sustained development; on average, they gained 0.28 age-equivalent score points per month (confidence interval 0.17-0.38). Apart from common (63%) cervical spinal stenosis, neuroimaging revealed unspecific, non-progressive abnormalities (i.e., mild brain atrophy, white matter lesions). In summary, MLII is associated with profound developmental impairment, but not with neurodegeneration and neurocognitive decline.

Indexed as

adaptive behaviourCNSdevelopmentimagingMLMLIIMRImucolipidosisnatural historyneurocognition

Identifiers

PMID37373807
PMCPMC10299287
OpenAlexW4381140681

What OpenQuestion holds

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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.