Evidence map›Paper›PMID 35950143›Full record

ArticleCase reports in dermatology

A Young Boy with Brittle Hair.

Nassim Tootoonchi, Vahideh Azhari, Zahra Razavi, Shadab Seraji, Nika Kianfar, Hamidreza Mahmoudi, Maryam Daneshpazooh

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 58% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. A Case of Isolated Trichothiodystrophy.Indian dermatology online journal · 2026
    Article
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

7 authors at 1 institution in 1 country.

Nassim TootoonchiDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Vahideh AzhariDepartment of Dermatopathology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Zahra RazaviDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Shadab SerajiDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Nika KianfarDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Hamidreza MahmoudiDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Maryam DaneshpazoohDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Razi Hospital · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trichothiodystrophy (TTD) is a rare multisystem disorder with an autosomal recessive mode of inheritance. TTD presentations vary from only hair abnormalities like brittle, fragile hair to physical and mental retardation. Mutations of DNA repair genes have been identified as responsible for the disease. A 5-year-old boy presented with sparse, short, and brittle hair to our clinic. He was born to consanguineous parents. Trichoscopy and light microscopy revealed broken hairs with no specific shaft defect. Due to the inaccessibility of the polarized microscopy, a bedside technique was employed. We used a polarized dermatoscope and a mirror in order of achieving transillumination of the hair shafts, which revealed striking bright and dark bands. These bands are referred to as "tiger tail," which is the pathognomonic sign of TTD. Subsequent polarizing microscopy also confirmed the clinical diagnosis. This highlighted a feasible method for observing the tiger tail, which expanded the known clinical diagnostic tools of TTD.

Indexed as

Autosomal recessiveBrittle hairPolarized lightTrichothiodystrophy

Identifiers

PMID35950143
PMCPMC9294941
OpenAlexW4283693933

What OpenQuestion 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 OpenQuestion graph.