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Record W4409792809 · doi:10.70962/cis2025abstract.153

Two Siblings with Possible Concurrent Atypical Papillon-Lefèvre Syndrome (PLS) and Activated Phosphoinositide 3-kinase Delta Syndrome 1 (APDS1)

2025· article· en· W4409792809 on OpenAlexaff
Luis Murguía-Favela, Michele Ramien, Renée Perrier

Bibliographic record

VenueJournal of Human Immunity · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer-related molecular mechanisms research
Canadian institutionsAlberta Children's HospitalUniversity of Calgary
Fundersnot available
KeywordsKinaseMedicineGastroenterologyInternal medicineChemistryBiochemistry

Abstract

fetched live from OpenAlex

PLS is an autosomal recessive disorder with palmoplantar hyperkeratosis, early-onset destructive periodontitis, and premature tooth loss, caused by mutations in CTSC leading to deficiency of cathepsin C. APDS1 is an autosomal dominant disorder due to heterozygous gain-of-function mutations in PIK3CD causing increased PI3K/mTOR/AKT intracellular signaling. We present 2 siblings with an atypical presentation in which both disorders may be coexisting. P1 is an 18-year-old male with palmoplantar erythema and hyperkeratosis since early childhood without periodontitis or dentition issues. At 16, he presented in ARDS and a CT chest showing multifocal consolidation, early cavitation, and a pattern suspicious for chronic hypersensitivity pneumonitis from the retinoid dermatological treatment. All infectious investigations were negative. He had lymphopenia and low IgG and IgM. He improved after methylprednisolone pulses and remained asymptomatic for 7 months when he had hypoxemia and a repeat CT showing multifocal nodular opacities and splenomegaly. EBV viral load was high. Despite a course of high-dose steroids, his symptoms and CT worsened with multifocal round opacities and nodules. An open lung biopsy showed histiocytes, CD4+ T cells, and B cells obliterating the normal lung architecture with areas of necrosis and positive EBER staining. Genetic testing showed compound heterozygosity for 2 CTSC variants (a pathogenic and a VUS), heterozygous pathogenic variant in FLG, and heterozygous VUS in PIK3CD. He was treated with rituximab clearing EBV and is on sirolimus. He is asymptomatic but with progressive T cell lymphopenia. P2 is 19 years old and has palmoplantar erythema and hyperkeratosis but no history of severe infections or periodontic disease. He has normal IgGAME and normal T/B/NK cell subsets. Genetic testing revealed the same variants as P1. They are adopted and thus have no known family history and no possibility for variant segregation or verification of cis vs. trans for CTSC variants. There are no reports of PLS without periodontitis. The skin manifestations in our patients are characteristic. The FLG variant may be contributing. Functional validation of the PIK3CD missense variant is pending. Tools predict a deleterious change in the protein; it is not in gnomAD and is located near the hotspot for mutations in APDS1.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.005
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.005
Threshold uncertainty score0.013

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.005
Meta-epidemiology (narrow)0.0030.002
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0020.002
Scholarly communication0.0010.002
Open science0.0020.003
Research integrity0.0050.004
Insufficient payload (model declined to judge)0.0040.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.010
GPT teacher head0.296
Teacher spread0.286 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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