Evidence map›Paper›PMID 37828451›Full record

ArticleBMC pediatrics2023

Zimmermann-Laband syndrome and infantile systemic hyalinosis: an enigma with two separate terms with overlapping features: a case report.

Fatemeh Owlia, Alireza Navabazam, Mohammad-Hasan Akhavan-Karbasi, Mohammad Moein Derakhshan Barjoei

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC pediatrics, 2023. 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
0.4field-weighted citation impact, top 28% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

4 authors at 1 institution in 1 country.

Fatemeh OwliaDepartment of Oral and Maxillofacial Medicine, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Alireza NavabazamDepartment of Oral and Maxillofacial Surgery, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Mohammad-Hasan Akhavan-KarbasiDepartment of Oral and Maxillofacial Medicine, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Mohammad Moein Derakhshan BarjoeiDentistry student, Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. mmdb1378@gmail.com.ORCID http://orcid.org/0000-0002-9653-8459
Shahid Sadoughi University of Medical Sciences and Health Services · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundZimmermann-Laband Syndrome (ZLS) and infantile systemic hyalinosis (ISH) are rare genetic disorders. They are characterized by various spectrum manifestations. In spite of other case reports, this case with features of both syndromes was reported by oral medicine specialists and oral and maxillofacial surgeons. CASE PRESENTATION: In this study, we reported an 18-months old female patient with gingival overgrowth. This phenomenon completely embedded all the erupted teeth. In this case, the presence of multiple papulonodular cutaneous lesions is a newly observed aspect that has rarely been reported in the existing literature. Gingival overgrowth was excised under general anesthesia. At six months of follow-up after surgery, mastication and breathing problems were improved. Aesthetic aspects were ameliorated in terms of gingival appearance.

conclusionsTo date, due to the ambiguous presentations, both syndromes remain an enigma for specialists. A timely diagnosis could be crucial for prognosis and preventing severe further surcharge. Dentists could play an important role in the diagnosis of rare disorders.

Indexed as

Abnormalities, MultipleCraniofacial AbnormalitiesFibromatosis, GingivalHyaline Fibromatosis SyndromeFemaleHand Deformities, CongenitalHumansInfantCase reportGingival enlargementInfantile systemic hyalinosisPapulonodular lesionsZimmermann-Laband Syndrome

Identifiers

PMID37828451
PMCPMC10571462
OpenAlexW4387598053

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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.