Evidence map›Paper›PMID 40215399›Full record

ArticleJournal of investigative medicine high impact case reports

Unmasking Cystic Fibrosis in Adulthood, a Case Report.

Malina Mohtadi, Ruba Habib, Abraam Rezkalla, George Horani, Radhika Tailor, Patrick Michael

Abstract readCase Reports
In one paragraph

Article in Journal of investigative medicine high impact case reports. 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
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.

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

6 authors.

Malina MohtadiSt. Joseph's University Medical Center, Internal Medicine, Paterson, NJ, USA.ORCID 0000-0003-2012-9939
Ruba HabibSt. Joseph's University Medical Center, Internal Medicine, Paterson, NJ, USA.
Abraam RezkallaSt. Joseph's University Medical Center, Internal Medicine, Paterson, NJ, USA.
George HoraniSt. Joseph's University Medical Center, Pulmonary and Critical Care, Paterson, NJ, USA.
Radhika TailorSt. Joseph's University Medical Center, Internal Medicine, Paterson, NJ, USA.
Patrick MichaelSt. Joseph's University Medical Center, Internal Medicine, Paterson, NJ, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is a genetic disorder typically diagnosed in early childhood, caused by mutations in the cystic fibrosis transmembrane conductance regulator gene, leading to thick mucus accumulation in the lungs, pancreas, and other organs. While most diagnoses occur in childhood, a growing number of cases are being identified in adulthood, presenting unique challenges for recognition and management. This case highlights a 37-year-old patient diagnosed with CF after presenting with chronic respiratory symptoms, and weight loss. Late diagnosis of CF remains rare but can delay appropriate treatment, potentially impacting long-term outcomes.

Indexed as

Cystic FibrosisAdultCystic Fibrosis Transmembrane Conductance RegulatorDelayed DiagnosisHumansMutationWeight LossCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorCFTR genechronic respiratory infectionscystic fibrosispancreatic insufficiency

Identifiers

PMID40215399
PMCPMC12033639

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.