Evidence map›Paper›PMID 38021743›Full record

ArticleCureus2023

Glycogen Storage Disease Type I With Hypercalcemia in an Infant: A Case Report.

Aziza Elouali, Chaimae N'joumi, Amal Bennani, Maria Rkain, Abdeladim Babakhouya

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2023. 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
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Aziza EloualiDepartment of Pediatrics, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, MAR.
Chaimae N'joumiDepartment of Pediatrics, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, MAR.
Amal BennaniDepartment of Anatomic Pathology, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, MAR.
Maria RkainDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, MAR.
Abdeladim BabakhouyaDepartment of Pediatrics, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, MAR.
Centre Hospitalier Universitaire Mohammed VI · MAMohamed I University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycogen storage disease type I (GSDI) is an uncommon condition resulting from a deficiency or absence of glucose-6-phosphatase, a key enzyme in regulating blood glucose levels. In this report, we describe a two-month-old girl diagnosed with GSDI who presented to the emergency department in a tertiary care hospital for irritability, excessive crying, and hyperventilation. She was found to have hepatomegaly and hypoglycemia. Laboratory investigations showed high levels of triglycerides, lactic acid, uric acid, and calcium. The combination of hypertriglyceridemia, hypoglycemia, and hepatomegaly should alert neonatologists and pediatricians to consider GSDI in the diagnosis. Hypercalcemia arose as an unknown problem in GSDI patients and should be considered during acute attacks.

Indexed as

case reportglycogen storage diseaseglycogen storage disease type ihypercalcemiahypertriglyceridemiametabolic decompensation

Identifiers

PMID38021743
PMCPMC10640896
OpenAlexW4387612814

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.