Evidence map›Paper›PMID 25161792›Full record

ArticleCase reports in pediatrics2014

The value of family history in diagnosing primary immunodeficiency disorders.

Mohamed A Hendaus, Ahmad Alhammadi, Mehdi M Adeli, Fawzia Al-Yafei

Abstract read
In one paragraph

Article in Case reports in pediatrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Navigating primary and secondary immunodeficiency intersections: how to find IEI hidden within SID.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2026
    Review
  2. Article
  3. 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.

Mohamed A HendausDepartment of Pediatrics, Section of General Pediatrics, Hamad Medical Corporation, Doha, Qatar.ORCID 0000-0001-9900-237X
Ahmad AlhammadiDepartment of Pediatrics, Section of General Pediatrics, Hamad Medical Corporation, Doha, Qatar ; Weill Cornell Medical College, Doha, Qatar.
Mehdi M AdeliWeill Cornell Medical College, Doha, Qatar ; Department of Pediatrics, Allergy and Immunology Section, Hamad Medical Corporation, Doha, Qatar.ORCID 0000-0002-3051-3080
Fawzia Al-YafeiDepartment of Pediatrics, Endocrinology Section, Hamad Medical Corporation, Doha, Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eliciting proper family medical history is critical in decreasing morbidity and mortality in patients with primary immunodeficiency disorders (PIDs). Communities with a common practice of consanguinity have a high rate of PIDs. We are presenting 2 cases where digging deeply into the family medical history resulted in the diagnosis of Omenn syndrome, a possibly fatal entity if not managed in a reasonable period.

Identifiers

PMID25161792
PMCPMC4137698

What OpenQuestion holds

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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.