Evidence map›Paper›PMID 42643713›Full record

ReviewIntractable & rare diseases research2026

Phenotypic variability of Fragile-X syndrome in Asian population: A systematic review.

Christina L Minar Napitupulu, Jeslyn Tengkawan, Agustini Utari, Tri Indah Winarni, Nydia Rena Benita Sihombing

Abstract readReview
In one paragraph

Review in Intractable & rare diseases research, 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

5 authors.

Christina L Minar NapitupuluMaster of Biomedical Sciences majoring in Genetic Counselling, Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia.
Jeslyn TengkawanDepartment of Pediatrics, Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia.
Agustini UtariDepartment of Pediatrics, Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia.
Tri Indah WinarniCommunity Genetic Research Center (ComGenRC), Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia.
Nydia Rena Benita SihombingCommunity Genetic Research Center (ComGenRC), Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the most common genetic cause of inherited intellectual disabilities. Individuals with full mutation of FXS exhibit physical and behavioral symptoms in addition to other comorbidities. The clinical features of FXS have been widely studied in Caucasians; however, they remain limited in the Asian population. This study aimed to characterize the spectrum and variability of physical and behavioral phenotypes in Asian populations. A total of 5,830 studies from the PubMed, ScienceDirect, Scopus, and Cochrane/CENTRAL databases were screened using the Covidence software. We identified FXS-specific research studies conducted in Asia that reported the clinical characteristics of individuals with FXS. This review summarizes 51 studies from different Asian regions. The frequently reported physical characteristics were large and prominent ears (72.63%), an elongated face (57.49%), and macroorchidism (45.21%). The three most prevalent behavioral characteristics were intellectual disability (ID), hyperactivity, and social withdrawal, reported in 99%, 77%, and 55% of all cases, respectively. Our findings show that the physical characteristics of FXS are variable in the Asian group but similar to those in other populations and are not recommended for early recognition. Individuals with intellectual disabilities, especially when combined with autism spectrum disorders and large prominent ears, are suggestive of further genetic testing for FXS.

Indexed as

behaviorFragile X syndromeintellectual disabilityphenotype

Identifiers

PMID42643713
PMCPMC13504694

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Registered trials

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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.