Evidence map›Paper›PMID 37121747›Full record

ArticleInternal medicine (Tokyo, Japan)2024

Late-onset Wilson Disease in a Patient Followed-up for Nonalcoholic Fatty Liver Disease.

Takeharu Asano, Shuhei Yoshikawa, Keita Matsumoto, Hitomi Kashima, Yudai Koito, Takaya Miura, Yuko Takahashi, Rumiko Tsuboi, Takehiro Ishii, Haruka Otake and 6 more

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2024. 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
0.2field-weighted citation impact, top 54% 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. 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

16 authors at 1 institution in 1 country.

Takeharu AsanoDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Shuhei YoshikawaDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Keita MatsumotoDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Hitomi KashimaDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Yudai KoitoDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Takaya MiuraDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Yuko TakahashiDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Rumiko TsuboiDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Takehiro IshiiDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Haruka OtakeDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Takeshi UeharaDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Masanari SekineDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Satohiro MatsumotoDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Shinichi AsabeDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Hiroyuki MiyataniDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Hirosato MashimaDepartment of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan.
Jichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 73-year-old woman was referred to our hospital for persistent liver dysfunction. When the patient was 45 years old, her youngest sister had been diagnosed with Wilson disease (WD). The patient therefore underwent several family screening tests, all of which were unremarkable. She had an annual medical checkup and was diagnosed with liver dysfunction and fatty liver at 68 years old. A liver biopsy and genetic testing were performed, and she was diagnosed with WD; chelation therapy was then initiated. In patients with hepatic disorders and a family history of WD, multiple medical examinations should be conducted, as the development of WD is possible regardless of age.

Indexed as

Hepatolenticular DegenerationNon-alcoholic Fatty Liver DiseaseAgedCopperFemaleGenetic TestingHumansMiddle AgedPatientsCopperATP7B genelate-onsetnonalcoholic fatty liver diseaseWilson disease

Identifiers

PMID37121747
PMCPMC10824639
OpenAlexW4367276467

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.