Evidence map›Paper›PMID 37091681›Full record

ArticleOxford medical case reports2023

Late diagnosis of tuberous sclerosis: a case report.

Luis F Domínguez-Valdez, Jaime E Hernández-Utrera, Iliana N Chávez-Sánchez, Ana L Peralta-Amaro, Melina J Talin-Bosquez, Luis A García-Pedraza, Carlos A Hernández-Jiménez, Diana K Delgado-Carmona, Abraham E Gracia-Ramos

Open access · goldAbstract readCase Reports
In one paragraph

Article in Oxford medical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
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

9 authors at 4 institutions in 1 country.

Luis F Domínguez-ValdezDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Jaime E Hernández-UtreraDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Iliana N Chávez-SánchezDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Ana L Peralta-AmaroDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Melina J Talin-BosquezDepartamento de Cardiología, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Luis A García-PedrazaDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Carlos A Hernández-JiménezDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Diana K Delgado-CarmonaDepartamento de Medicina Interna, UMAE Hospital de Especialidades 'Dr. Antonio Fraga Mouret', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Abraham E Gracia-RamosDepartamento de Medicina Interna, UMAE Hospital General 'Dr. Gaudencio González Garza', Centro Médico Nacional 'La Raza', Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Hospital de Especialidades · MXCentro Médico Nacional La Raza · MXMexican Social Security Institute · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by the formation of hamartomas in organ systems such as the brain, skin, kidneys and lungs. Patients with TSC are usually diagnosed early in life. However, in some cases, the diagnosis is delayed until adulthood because various manifestations occur at various times throughout an individual's life. In this regard, we present the case of a female patient diagnosed at the beginning of the seventh decade of life. The patient had a history of seizures and showed clinical findings on the skin (facial angiofibromas, ungual fibromas, 'Confetti-like' skin lesions, shagreen patch), brain (cortical tubers), heart (cardiac rhabdomyomas), kidneys (angiomyolipomas) and a positive genetic test for mutations in TSC2, fulfilling the diagnostic criteria. We compared the differences between manifestations in patients diagnosed during childhood and adulthood. Knowledge of the clinical spectrum of TSC allows early identification.

Identifiers

PMID37091681
PMCPMC10120429
OpenAlexW4366775190

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.