Evidence map›Paper›PMID 35464534›Full record

ArticleCureus2022

Transient Cytopenias as a Rare Presentation of Classic Galactosemia.

Maria Gianniki, Irini Nikaina, Georgia Avgerinou, Christina Kanaka-Gantenbein, Tania Siahanidou

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

Article in Cureus, 2022. 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
0.8field-weighted citation impact, top 28% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

5 authors at 1 institution in 1 country.

Maria GiannikiFirst Department of Pediatrics, National and Kapodistrian University of Athens, Athens, GRC.
Irini NikainaFirst Department of Pediatrics, National and Kapodistrian University of Athens, Athens, GRC.
Georgia AvgerinouFirst Department of Pediatrics, National and Kapodistrian University of Athens, Athens, GRC.
Christina Kanaka-GantenbeinFirst Department of Pediatrics, National and Kapodistrian University of Athens, Athens, GRC.
Tania SiahanidouFirst Department of Pediatrics, National and Kapodistrian University of Athens, Athens, GRC.
National and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although galactosemia can be detected through neonatal screening, some cases are characterized by rapid and severe presentation before screening results become available. We report the case of a neonate with classic galactosemia presenting with acute liver failure and cytopenias (thrombocytopenia, anemia, and neutropenia). Neonatal screening results showed increased galactose and phenylalanine levels. The diagnosis of galactosemia was confirmed by the measurement of galactose-1-phosphate uridyltransferase (GALT) activity in erythrocytes. Two mutations of the

Indexed as

cytopeniasgalactosemialiver failurenewbornthrombocytopenia

Identifiers

PMID35464534
PMCPMC8998154
OpenAlexW4220826739

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.