Evidence map›Paper›PMID 41356612›Full record

ArticleHealth science reports2025

The Multifactorial Causes of Down Syndrome During Pregnancy: A Narrative Review of Genetic, Environmental, and Maternal Influences.

Md Sohel Rana, Mst Morium Parvin, Md Tariqul Islam

Abstract read
In one paragraph

Article in Health science reports, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Md Sohel RanaDepartment of Biochemistry and Biotechnology Khwaja Yunus Ali University Sirajganj Bangladesh.
Mst Morium ParvinDepartment of Biochemistry and Biotechnology Khwaja Yunus Ali University Sirajganj Bangladesh.
Md Tariqul IslamDepartment of Biochemistry and Biotechnology Khwaja Yunus Ali University Sirajganj Bangladesh.ORCID https://orcid.org/0000-0003-4056-8760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Chromosomal nondisjunction is the primary etiology of Down syndrome; however, genetic variations, environmental causes, and maternal etiologies also contribute to a great extent. The objective of this review is to evaluate these multifaceted factors during pregnancy. Methods: A comprehensive review of the literature of research and epidemiology was performed to examine the environmental factors, genetic factors, and clinical variables that influence Down syndrome. The research concludes with a discussion of new prenatal testing methods, the danger presented by increased maternal age, and how such issues impact the affected families. Results: The genetic polymorphisms were associated with a higher rate of chromosomal nondisjunction, particularly in the genes for folate metabolism, including MTHFR, RFC1, and MTHFD. These factors like education level of the mother, income, and access to prenatal care can raise or lower Down syndrome. People born with problems, like heart problems or problems with their intestines, tend to have problems with their bodies and minds also. The article also mentions how hard it is for parents to deal with the emotional weight of having a prenatal diagnosis and how common this condition is in different racial and cultural groups. Conclusion: Down syndrome is still a complicated illness caused by genetics, the environment, and the mother. With enhanced prenatal screening to detect problems before birth, families still encounter moral and ethical dilemmas. We need to learn more through further research on genetic modifiers, how the environment affects them, and how they affect health in the long run. A deeper understanding of these concerns will make prenatal counseling more robust and more effective treatment procedures for individuals with Down syndrome.

Indexed as

chromosomal nondisjunctionDown syndromegenetic polymorphisms

Identifiers

PMID41356612
PMCPMC12678631

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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.