Evidence map›Paper›PMID 37025736›Full record

ArticleCureus2023

A Previously Undiagnosed Case of Alkaptonuria in an 80-Year-Old Patient: A Case Report.

Mohit K Singh, Faisal A Memon, Smita A Deokar, Yash Achhapalia, Ganesh R Yeotiwad

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2023. 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
1.0field-weighted citation impact, top 27% 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
  2. 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

5 authors at 2 institutions in 2 countries.

Mohit K SinghBiochemistry, Hinduhrudaysamrat Balasaheb Thackarey (HBT) Medical College and Dr. R. N. Cooper Hospital, Mumbai, IND.
Faisal A MemonInternal Medicine, Hinduhrudaysamrat Balasaheb Thackarey (HBT) Medical College and Dr. R. N. Cooper Hospital, Mumbai, IND.
Smita A DeokarBiochemistry, Hinduhrudaysamrat Balasaheb Thackarey (HBT) Medical College and Dr. R. N. Cooper Hospital, Mumbai, IND.
Yash AchhapaliaSurgery, Liverpool University Hospital NHS Foundation Trust, Liverpool, GBR.
Ganesh R YeotiwadOrthopaedics, Hinduhrudaysamrat Balasaheb Thackarey (HBT) Medical College and Dr. R. N. Cooper Hospital, Mumbai, IND.
Aintree University Hospitals NHS Foundation Trust · GBCooper Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alkaptonuria is a rare genetic metabolic disorder of autosomal recessive inheritance characterised by the accumulation of homogentisic acid in the body. It is diagnosed upon identification of characteristic symptoms, using various biochemical investigations, radiographic pictures, and a variety of specialised tests. Here we are discussing the case of an 80-year-old female patient with incidental findings of alkaptonuria. It is crucial to understand the fundamental diagnostic investigations that can be used in low-income nations or facilities where investigations like genetic testing, gas chromatography, and mass spectrometry are not readily available for the diagnosis of alkaptonuria.

Indexed as

alkaptonuriaascorbic acidbiochemical testsgeneticshomogentisic acidnitisinoneochronosis

Identifiers

PMID37025736
PMCPMC10072848
OpenAlexW4323257228

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.