Evidence map›Paper›PMID 38199782›Full record

ReviewCold Spring Harbor molecular case studies2023

The diagnostic odyssey of a patient with dihydropyrimidinase deficiency: a case report and review of the literature.

Daniah Albokhari, Ohood Alharbi, Alyssa Blesson, Mahim Jain

Open access · diamondAbstract readReviewCase Reports
In one paragraph

Review in Cold Spring Harbor molecular case studies, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

4 authors at 2 institutions in 2 countries.

Daniah AlbokhariDepartment of Pediatrics, Taibah University College of Medicine, Medina 42353, Saudi Arabia.ORCID 0000-0001-7380-0760
Ohood AlharbiTaibah University College of Medicine, Medina 42353, Saudi Arabia.
Alyssa BlessonDepartment of Bone/Osteogenesis Imperfecta, Kennedy Krieger Institute, Baltimore, Maryland 21205, USA.
Mahim JainDepartment of Bone/Osteogenesis Imperfecta, Kennedy Krieger Institute, Baltimore, Maryland 21205, USA; jainm@kennedykrieger.org.
Kennedy Krieger Institute · USTaibah University · SA

Funding

Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
NICHD NIH HHS P50 HD103538
6 · The paper itself

Abstract

Dihydropyrimidinase (DHP) deficiency is an autosomal recessive metabolic disorder caused by biallelic pathogenic variants of

Indexed as

Metabolism, Inborn ErrorsDiphosphonatesGenetic TestingHumansPhenotypeDiphosphonatesarthrogryposis-like hand anomalydevelopmental stagnation at onset of seizuresdysphagiagastroesophageal refluxosteoporosis of vertebraeperiventricular leukomalaciaprofound global developmental delayslowly progressive spastic quadriparesis

Identifiers

PMID38199782
PMCPMC10815279
OpenAlexW4390711154

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.