Evidence map›Paper›PMID 27252793›Full record

ArticleJournal of radiology case reports2015

Idiopathic Arterial Calcification of Infancy: Case Report.

Tarek Hamed Attia, Mohamed Maisara Abd Alhamed, Mohamed Fouad Selim, Mohamed Salah Haggag, Diaa Fathalla

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Journal of radiology case reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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 3 institutions in 1 country.

Tarek Hamed AttiaDepartment of Pediatrics, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Mohamed Maisara Abd AlhamedDepartment of Pediatrics, Al-hammadi Hospital, Riyadh, Saudi Arabia.
Mohamed Fouad SelimDepartment of Obstetrics and Gynecology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Mohamed Salah HaggagDepartment of Radiology, Faculty of Medicine, Banha University, Banha, Egypt.
Diaa FathallaDepartment of cardiology, Faculty of Medicine, Tanta University, Tanta, Egypt.
Zagazig University · EGBenha University · EGTanta University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic arterial calcification of infancy is a rare autosomal recessive disease, characterized by deposition of calcium along the internal elastic membrane of arteries, accompanied by fibrous thickening of the intima which causes luminal narrowing. Here we are reporting a case of idiopathic arterial calcification of infancy in a Saudi female newborn of non-consanguineous pregnant woman who had polyhydramnios. The newborn baby had severe respiratory distress, systemic hypertension and persistent pulmonary hypertension of newborn. She was admitted to Neonatal Intensive Care Unit, where she was ventilated and proper treatment was provided. Molecular genetic testing was positive for mutations of ectonucleotide pyrophosphatase/phosphodiesterase1 gene which is reported in 80% of cases of Idiopathic arterial calcification of infancy. The baby died at about 5 month of age because of myocardial ischemia and cardiorespiratory arrest. Idiopathic Arterial Calcification of Infancy should be considered in any newborn who presented with persistent pulmonary hypertension of newborn, severe systemic hypertension and echogenic vessels on any radiological study. Calcifications of large and medium-sized arteries are important diagnostic finding.

Indexed as

Diagnosis, DifferentialFatal OutcomeFemaleHumansInfant, NewbornVascular Calcificationarterial calcification of infancyarterial calcificationsarteriesautosomal recessivecardiomyopathyCTIdiopathic arterial calcification of infancypolyhydramnios

Identifiers

PMID27252793
PMCPMC4871139
OpenAlexW2264214526

What OpenQuestion holds

Textmetadata
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.