Evidence map›Paper›PMID 32821314›Full record

ArticleThe Pan African medical journal2020

[An unusual case of cardiomyopathy showing carnitine palmitoyltransferase deficiency].

Imane Fetoui, Karima El Fakiri, Noureddine Rada, Ghizlane Draiss, Mohammed Bouskraoui

Open access · goldAbstract readCase Reports
In one paragraph

Article in The Pan African medical journal, 2020. 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, top 92% 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, 0 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.

Imane FetouiService de Pédiatrie, Hôpital Mère Enfant CHU Mohammed VI, Marrakech, Maroc.
Karima El FakiriService de Pédiatrie, Hôpital Mère Enfant CHU Mohammed VI, Marrakech, Maroc.
Noureddine RadaService de Pédiatrie, Hôpital Mère Enfant CHU Mohammed VI, Marrakech, Maroc.
Ghizlane DraissService de Pédiatrie, Hôpital Mère Enfant CHU Mohammed VI, Marrakech, Maroc.
Mohammed BouskraouiService de Pédiatrie, Hôpital Mère Enfant CHU Mohammed VI, Marrakech, Maroc.
Centre Hospitalier Universitaire Mohammed VI · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carnitine palmitoyltransferase deficiencies (CPD) are rare and caused by a defect in fatty acid oxidation. We here report the case of a 10-year-old patient with no particular previous history presenting with acute dyspnea associated with productive cough, fever and impaired general condition. The patient was polypneic with tachycardia, mitral systolic murmur and no sign of heart failure. Chest x-ray showed cardiomegaly and echocardiography revealed hypokinetic dilated cardiomyopathy. Carnitine palmitoyltransferase deficiency was diagnosed. Management was based on treatment for heart disease and strict hypopidic and hyperglucidic diet. Three months later, the patient presented with decompensated heart failure due to infection caused by antibiotic-resistant Aeromonas caviae identified in blood culture. CPD should be suspected in patients with dilated cardiomyopathy. This would enable early management which influences prognosis.

Indexed as

Aeromonas caviaeAnti-Bacterial AgentsCardiomyopathy, DilatedCarnitine O-PalmitoyltransferaseChildDrug Resistance, BacterialGram-Negative Bacterial InfectionsHeart FailureHumansMaleAnti-Bacterial AgentsCarnitine O-PalmitoyltransferaseAeromonas caviaeCardiomyopathycarnitine palmitoyl transférasechildren

Identifiers

PMID32821314
PMCPMC7406460
OpenAlexW3035910960

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.