Evidence map›Paper›PMID 41362562›Full record

ArticleCureus2025

Early-Onset Leukonychia as a Diagnostic Clue in Familial Hailey-Hailey Disease.

Assia El Bouhmadi, Hanane Rachadi, Bouchra Baghad, Fatima Zahra El Fatoiki, Soumiya Chiheb

Abstract readCase Reports
In one paragraph

Article in Cureus, 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
–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

5 authors.

Assia El BouhmadiDermatology, Ibn Rochd University Hospital Center, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, MAR.
Hanane RachadiDermatology, Ibn Rochd University Hospital Center, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, MAR.
Bouchra BaghadDermatology, Ibn Rochd University Hospital Center, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, MAR.
Fatima Zahra El FatoikiDermatology, Ibn Rochd University Hospital Center, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, MAR.
Soumiya ChihebDermatology, Ibn Rochd University Hospital Center, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hailey-Hailey disease (HHD) is a rare autosomal dominant genodermatosis characterized by recurrent intraepidermal blistering and erosions, most often affecting flexural and intertriginous areas. Although its clinical presentation is distinctive, the disease exhibits considerable variability and is often misdiagnosed, particularly in early or atypical forms. Nail involvement, historically considered absent, has recently been recognized as an underappreciated feature that may provide valuable diagnostic clues. We report a familial case of HHD spanning three generations, in which a single longitudinal leukonychia in the proband preceded the onset of typical skin lesions. The initial nail change, unassociated with trauma or systemic disease, prompted a detailed family history revealing recurrent erosive lesions in relatives. Months later, the proband developed painful, fissured, erythematous plaques in flexural regions, confirmed histologically as HHD. Treatment with topical calcineurin inhibitors, oral doxycycline, and ultraviolet B (UVB) phototherapy led to marked clinical improvement and reduced flare frequency, although the leukonychia remained unchanged. This case highlights the diagnostic importance of subtle nail findings in HHD. Early-onset or isolated leukonychia, often asymptomatic and easily overlooked, may precede cutaneous involvement and thus represent a valuable marker for early detection in at-risk individuals. Recognition of such signs can facilitate timely diagnosis, genetic counseling, and preventive management within affected families. Nail alterations in HHD appear long-lasting and independent of disease activity, underscoring their potential role as a stable phenotypic manifestation of this disorder. Early identification of these subtle nail changes can therefore improve patient outcomes by guiding early therapeutic intervention and reducing the delay in diagnosis often associated with this underrecognized condition.

Indexed as

genodermatosishailey-haileyhereditary dermatological disordersleukonychianail disorders

Identifiers

PMID41362562
PMCPMC12682309

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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.