Evidence map›Paper›PMID 33738777›Full record

ArticleActa neurologica Belgica2022

The clinical and paraclinical manifestations of tuberous sclerosis complex in children.

Mohammad Barzegar, Bita Poorshiri, Leila Yousefi, Sina Raeisi, Hassan Bakhtiary, Amir Eftekhari Milani, Zakiyeh Ebadi

Abstract read
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In one paragraph

Article in Acta neurologica Belgica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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.

Mohammad BarzegarPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. mm_barzegar@yahoo.com.ORCID http://orcid.org/0000-0002-5503-9039
Bita PoorshiriPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Leila YousefiMedical Radiation Sciences Research Group, Department of Radiology, Tabriz University of Medical Sciences, Tabriz, Iran.
Sina RaeisiPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hassan BakhtiaryPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Amir Eftekhari MilaniDepartment of Ophthalmology, Nikookary Eye Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Zakiyeh EbadiPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Tabriz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberous sclerosis complex (TSC) is an autosomal-dominant, multi-system, neurocutaneous disorder characterized by hamartomas in multiple organs. This study aimed to evaluate the clinical and paraclinical manifestations of children with TSC. The clinical and paraclinical characteristics of 79 children with TSC were evaluated and the possible correlations between the factors were calculated. Among the studied children which composed of 41 females (51.9%) and 38 males (48.1%), skin manifestations as hypopigmented macules as well as the brain involvement as cortical tubers in all (100%) cases, seizure in 74 (93.7%), and sub-ependymal nodules in 73 (92.4%) patients were the most common findings. The renal angiomyolipoma was diagnosed in 36 (70.6%) out of 51 patients. Subependymal giant cell astrocytoma in 25 (3/54%) out of 46 patients, retinal hamartoma in 15 (42.9%) out of 35 patients, and cardiac rhabdomyoma in 17 (41.3%) out of 46 patients were diagnosed. Furthermore, 50 (63.3%) out of 79 patients had psychological disorders that had a significant correlation with the prevalence of seizures (p = 0.002). Given the multi-systemic involvement of TSC, it is necessary that all organs of the patients even without any related clinical symptom or sign be examined regularly for proper therapeutic intervention and prevent disease progression. The growth of hamartomas in the brain and kidneys can be life-threatening; therefore, these organs have more importance to be regularly followed up and examined.

Indexed as

AngiomyolipomaAstrocytomaHamartomaKidney NeoplasmsTuberous SclerosisChildFemaleHumansMaleSeizuresChildrenClinical manifestationsParaclinical manifestationsTuberous sclerosis complex

Identifiers

PMID33738777
OpenAlexW3137079369

What OpenQuestion holds

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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.