Evidence map›Paper›PMID 38229774›Full record

ArticleCureus2023

Cluster Case of Prolidase Deficiency: Varied Clinical Presentations and Management in a Sibling Trio.

Saud Azhar, Palwasha Khan, Fahad Faizullah, Sohana Hakim, Madiha Aslam

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 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 29% 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

5 authors at 1 institution in 1 country.

Saud AzharInternal Medicine, Hayatabad Medical Complex Peshawar, Peshawar, PAK.
Palwasha KhanDermatology, Hayatabad Medical Complex Peshawar, Peshawar, PAK.
Fahad FaizullahDermatology, Hayatabad Medical Complex Peshawar, Peshawar, PAK.
Sohana HakimDermatology, Hayatabad Medical Complex Peshawar, Peshawar, PAK.
Madiha AslamDermatology, Hayatabad Medical Complex Peshawar, Peshawar, PAK.
Hayatabad Medical Complex · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolidase deficiency (PD) is an exceptionally rare autosomal recessive disorder characterized by impaired collagen degradation, leading to the accumulation of proline-containing dipeptides. We report a cluster case of three siblings aged 17, 19, and 20 years, comprising of two sisters and one brother, who presented with non-healing ulcers on their shins and feet along with facial features of hypertelorism, depressed nasal bridge, reduced intellectual function, and high-arched palate. History and clinical features were consistent with PD. Due to the rarity of the disease and low socioeconomic background of the patients, specialized investigations or treatments were either unavailable or inaccessible. Furthermore, surgical intervention was ill-advised. Despite these challenges, patients were treated using improvised tailored therapy using three different modalities and showed remarkable progress. The evaluation and management took place at the dermatology unit of Hayatabad Medical Complex in Peshawar, Pakistan.

Indexed as

autoimmune diseasecollagen degradationfacial malformationsfoot ulcernon-healing ulcerspepd geneprolidase deficiency

Identifiers

PMID38229774
PMCPMC10791084
OpenAlexW4389856969

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.