Evidence map›Paper›PMID 42548784›Full record

ArticleClinical case reports2026

Rare Coexistence of Familial Laryngo-Onycho-Cutaneous Syndrome (LOCS/Shabbir Syndrome) and Epidermolysis Bullosa With Multisystemic Involvement: A Case Series.

Zainab Rasheed, Muhammad Rashid, Usman Syed Mahmud, Muhammad Hassaan Javaid, Raghabendra Kumar Mahato, Zubaria Yaqoob

Abstract read
In one paragraph

Article in Clinical case reports, 2026. 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.

Zainab RasheedDepartment of ENT Shifa International Hospital Islamabad Pakistan.
Muhammad RashidDepartment of ENT Shifa International Hospital Islamabad Pakistan.
Usman Syed MahmudDepartment of ENT Shifa International Hospital Islamabad Pakistan.
Muhammad Hassaan JavaidDepartment of Medicine Shifa College of Medicine Islamabad Pakistan.ORCID https://orcid.org/0009-0000-1800-1800
Raghabendra Kumar MahatoGandaki Medical College Teaching Hospital and Research Center Pokhara Nepal.ORCID https://orcid.org/0009-0009-9434-1650
Zubaria YaqoobShifa International Hospitals Islamabad Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coexistence of LOCS and a broader EB phenotype within a single consanguineous family represents a unique instance of intra-familial phenotypic heterogeneity in LAMA3-related junctional epidermolysis bullosa. This highlights the importance of recognizing systemic manifestations, including urological and neurological complications, and underscores early diagnosis, multidisciplinary management, and genetic counseling.

Indexed as

consanguinityepidermolysis bullosajunctional EBLAMA3 mutationLaminin‐332Laryngo‐onycho‐cutaneous syndromephenotypic heterogeneityShabbir syndrome

Identifiers

PMID42548784
PMCPMC13429933

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.