Evidence map›Paper›PMID 42390629›Full record

ArticleJournal of community genetics2026

Genetic services in Pakistan: a review highlighting limitations and opportunities for improvement.

Abdul Khaliq, Abrar Hussain

Abstract readLetter
In one paragraph

Article in Journal of community genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Abdul KhaliqDepartment of Life Sciences, Lahore University of Management Sciences, Lahore, Pakistan. abdulkhaliq4242@gmail.com.
Abrar HussainDepartment of Biological Sciences, International Islamic University Islamabad, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic services, including genetic testing and genetic counseling, are essential components of modern healthcare and play a critical role in diagnosis, management, and prevention of inherited disorders. In Pakistan, the burden of genetic disorders is substantially increased by high rates of consanguinity, limited public awareness, inadequate healthcare infrastructure, and the absence of formal genetic counseling services. This review evaluates the current status of genetic services in Pakistan, focusing on genetic testing facilities, genetic counseling, healthcare infrastructure, workforce limitations, ethical considerations, and recent initiatives aimed at improving genomic healthcare delivery. A narrative review of the literature was conducted using national and international studies related to medical genetics and genetic counseling. The findings indicate that genetic services in Pakistan remain limited, costly, and largely inaccessible within the public healthcare sector. Advanced diagnostic technologies, including whole exome/genome sequencing (WES/WGS), and non-invasive prenatal testing (NIPT), are mostly outsourced internationally, restricting access for much of the population. Furthermore, Pakistan lacks formal postgraduate training programs and professional accreditation systems for genetic counselors (GCs). Recent efforts by the Pakistani Society of Medical Genetics and Genomics (PSMG), including telehealth genetic clinics, educational programs, and international collaborations, represent important steps toward improving genetic services in resource-limited settings. This review emphasizes that establishing a national genomics policy, expanding local diagnostic infrastructure, and developing accredited genetic counseling training programs are urgently needed for the sustainable integration of genomic medicine into Pakistan's healthcare system.

Indexed as

Genetic counselingGenetic servicesGenomics policyInherited disordersMedical geneticsPakistanPublic health

Identifiers

PMID42390629
PMCPMC13328606

What Socratic holds

Textmetadata
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 Socratic graph.