Evidence map›Paper›PMID 39926682›Full record

ArticlePakistan journal of medical sciences2025

Spectrum of different categories of Primary Immunodeficiency Disorders diagnosed at Children Hospital.

Aisha Iftikhar, Mobeen Nazar, Adeela Chaudry, Ahmad Qaisar

Abstract read
In one paragraph

Article in Pakistan journal of medical sciences, 2025. 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
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1 · What the graph read from it

What it found

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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

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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.

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

4 authors.

Aisha IftikharAisha Iftikhar, FCPS, Department of Pediatrics, University of Child Health Sciences, Lahore, Pakistan.
Mobeen NazarMobeen Nazar, FCPS, Department of Pediatrics, University of Child Health Sciences, Lahore, Pakistan.
Adeela ChaudryAdeela Chaudry, FCPS, Department of Pediatrics, University of Child Health Sciences, Lahore, Pakistan.
Ahmad QaisarAhmad Qaisar, MBBS, FMH College of Medicine and Dentistry, Lahore, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine the frequency and spectrum of different categories of Primary immunodeficiency disorders (PIDD). Methodology: This was a prospective, observational analytical study, conducted in the Pediatric Medicine Department, University of Child Health Sciences (UCHS) from January 2021 to January 2023.We recruited 81 patients, initially suspected based on Jeffrey Modell Foundation(JMF) warning signs, followed by detailed evaluation. Descriptive statistics were applied. Results: Male patients exceeded female (47: 31). Median age of presentation was 17 months. Median diagnostic delay was 10.5 months. Need of I/V antibiotics was the most frequent JMF warning sign (88.5%). Consanguinity, previous hospital admissions, family history and sibling death were present in 80%, 78%, 54%, 37% of cases respectively. The most conspicuous clinical feature was persistent or recurrent thrush (51%). Patients were categorized into six main groups: B-Cell defect (29.5%), SCID (24.4%), CID (14.1%), T-Cell defect (12.8 %), Phagocytic defect (11.5%) and NK deficiency (7.7%). Main bulk of patients 37 (47.4 %) were in age-group up to one year. Most common site of infection was recurrent pneumonia (76%) and the least was septic arthritis (5.1%). Conclusion: PIDD should no longer be considered a rarity. B-Cell defect is the most common while earliest to diagnose are SCID and LAD. International health authorities should advocate EQUITABLE utilization of genetic testing across the globe.

Indexed as

B-Cell defectFlow cytometryNatural killer cell deficiencyPhagocytic defectPrimary immunodeficiencySevere combined immunodeficiency

Identifiers

PMID39926682
PMCPMC11803810

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