Evidence map›Paper›PMID 42103326›Full record

ArticleThe Journal of international medical research2026

Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report.

Nabeha Haytham Alibrahim, Ayham Qatza, Abdullah Dukhan, Mohammad Almoustafa, Thaer Douri

Abstract readCase Reports
In one paragraph

Article in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Nabeha Haytham AlibrahimDepartment of Dermatology, National Hama Hospital, Syria.
Ayham QatzaFaculty of Medicine, Hama University, Syria.ORCID 0009-0001-0424-2037
Abdullah DukhanFaculty of Medicine, Hama University, Syria.
Mohammad AlmoustafaFaculty of Medicine, Hama University, Syria.
Thaer DouriDepartment of Dermatology, Hama University, Hama, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atrichia with papular lesions is a rare autosomal recessive genodermatosis characterized by complete, irreversible hair loss that typically begins in infancy and is often misdiagnosed due to phenotypic similarity to other forms of alopecia. A 4-year-old male patient presented with complete hair loss since infancy, with absent eyebrows and eyelashes and no evidence of regrowth. His younger sister exhibited identical features, consistent with a history of consanguinity in the family. Physical examination revealed smooth skin and multiple firm, painless, keratotic papules (2-3 mm) on the scalp and cheeks. A 4-mm punch biopsy demonstrated an absence of mature hair follicles, replaced by keratin-filled cysts without significant inflammation. These histopathological findings, together with the clinical presentation, supported a high-likelihood diagnosis of atrichia with papular lesions. Established diagnostic criteria supported this assessment even in the absence of human hairless gene testing, particularly in consanguineous families in resource-limited settings. The family received counseling regarding the irreversible nature of the condition and was offered psychological support. This case highlights the diagnostic challenges encountered in resource-limited settings and proposes a clinical framework that prioritizes heightened clinical awareness and targeted screening in high-risk populations, including consanguineous families with a history of atrichia with papular lesions or other autosomal recessive skin disorders.

Indexed as

AlopeciaChild, PreschoolConsanguinityFemaleHair FollicleHumansMalePedigreeSiblingsSkin Diseases, VesiculobullousSyriaatrichia congenitaAtrichia with papular lesionscase reporthair loss

Identifiers

PMID42103326
PMCPMC13167302

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