Evidence map›Paper›PMID 37954711›Full record

ReviewCureus2023

The Impact of Artificial Intelligence on Optimizing Diagnosis and Treatment Plans for Rare Genetic Disorders.

Shenouda Abdallah, Mouhammad Sharifa, Mohammed Khaleel I Kh Almadhoun, Muhammad Muneeb Khawar, Unzla Shaikh, Khaled M Balabel, Inam Saleh, Amima Manzoor, Arun Kumar Mandal, Osatohanmwen Ekomwereren and 2 more

Abstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. Genomics in Health and Biomedicine.Advances in experimental medicine and biology · 2026
    Review
  15. Insights into the Diagnosis, Treatment, and Management of Prion Diseases.CNS & neurological disorders drug targets · 2026
    Review
  16. Review
  17. Personalized Medicine in Treating Rare Genetic Disorders: A Review.Journal of pharmacy & bioallied sciences · 2025
    Review
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  19. 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

12 authors.

Shenouda AbdallahSurgery, Jaber Al Ahmad Al Jaber Al Sabah Hospital, Kuwait City, KWT.
Mouhammad SharifaMedicine, University of Aleppo, Aleppo, SYR.
Mohammed Khaleel I Kh AlmadhounMedicine and Surgery, Mutah University, Karak, JOR.
Muhammad Muneeb KhawarInternal Medicine, Mayo Hospital, Lahore, PAK.
Unzla ShaikhInternal Medicine, Liaquat University of Medical and Health Sciences, Hyderabad, PAK.
Khaled M BalabelInternal Medicine, Saint Joseph Regional Center, Mishwaka, USA.
Inam SalehPediatrics, University of Kentucky College of Medicine, Lexington, USA.
Amima ManzoorInternal Medicine, Jinnah Sindh Medical University, Karachi, PAK.
Arun Kumar MandalGeneral Medicine, Mahawai Basic Hospital/The Oda Foundation, Kalikot, NPL.
Osatohanmwen EkomwererenTrauma and Orthopaedics, Royal Shrewsbury Hospital, Shrewsbury and Telford Hospital NHS Trust, Shrewsbury, GBR.
Wai Mon KhineInternal Medicine, Caribbean Medical School, St. Georges, GRD.
Oluwaseyi T OyelajaSurgery, Wyckoff Heights Hospital, Brooklyn, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare genetic disorders (RDs), characterized by their low prevalence and diagnostic complexities, present significant challenges to healthcare systems. This article explores the transformative impact of artificial intelligence (AI) and machine learning (ML) in addressing these challenges. It emphasizes the need for accurate and early diagnosis of RDs, often hindered by genetic and clinical heterogeneity. This article discusses how AI and ML are reshaping healthcare, providing examples of their effectiveness in disease diagnosis, prognosis, image analysis, and drug repurposing. It highlights AI's ability to efficiently analyze extensive datasets and expedite diagnosis, showcasing case studies like Face2Gene. Furthermore, the article explores how AI tailors treatment plans for RDs, leveraging ML and deep learning (DL) to create personalized therapeutic regimens. It emphasizes AI's role in drug discovery, including the identification of potential candidates for rare disease treatments. Challenges and limitations related to AI in healthcare, including ethical, legal, technical, and human aspects, are addressed. This article underscores the importance of data ethics, privacy, and algorithmic fairness, as well as the need for standardized evaluation techniques and transparency in AI research. It highlights second-generation AI systems that prioritize patient-centric care, efficient patient recruitment for clinical trials, and the significance of high-quality data. The integration of AI with telemedicine, the growth of health databases, and the potential for personalized therapeutic recommendations are identified as promising directions for the field. In summary, this article provides a comprehensive exploration of how AI and ML are revolutionizing the diagnosis and treatment of RDs, addressing challenges while considering ethical implications in this rapidly evolving healthcare landscape.

Indexed as

deep learning artificial intelligencegenetic basis of congenital heart diseasegenetic syndromesgenetic variantrare genetic diseases

Identifiers

PMID37954711
PMCPMC10636514

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.