Evidence map›Paper›PMID 35261770›Full record

ArticleClinical case reports2022

Atypical presentation of adenosine deaminase 2 deficiency with bi-allelic ADA2 mutation.

Reem Al-Shaikh, Dimah Alnowaiser, Abdul Ali Peer-Zada, Awatif Almutairi, Hamza Alghamdi

Erratum issuedAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Mimics and challenging presentations of DADA2.Clinical and experimental immunology · 2025
    Review
  2. Article
  3. Erratum:  Corrigendum.Clinical case reports · 2022
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Reem Al-ShaikhGeneral Pediatrics Department, Allergy and Immunology Section Children's Specialized Hospital King Fahad Medical City Riyadh Saudi Arabia.
Dimah AlnowaiserGeneral Pediatrics Department, Allergy and Immunology Section Children's Specialized Hospital King Fahad Medical City Riyadh Saudi Arabia.
Abdul Ali Peer-ZadaMolecular Pathology (Genetics) Section, Pathology and Clinical Laboratory Medicine Administration King Fahad Medical City Riyadh Saudi Arabia.ORCID https://orcid.org/0000-0002-9172-712X
Awatif AlmutairiGeneral Pediatrics Department, Allergy and Immunology Section Children's Specialized Hospital King Fahad Medical City Riyadh Saudi Arabia.
Hamza AlghamdiGeneral Pediatrics Department, Allergy and Immunology Section Children's Specialized Hospital King Fahad Medical City Riyadh Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we report a case of VAIHS with atypical clinical presentation of perianal abscess, fistula fever, and bi-cytopenia including pathogenic ADA2 mutation suggesting that ADA2 deficiency be considered as a differential diagnosis of enlarging cutaneous abscess with no evidence of wound healing in the setting of leukopenia and neutropenia.

Indexed as

ADA2autoinflammationautosomal recessive vasculitishematologic defects syndromeimmunodeficiency

Identifiers

PMID35261770
PMCPMC8888922

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.