Evidence map›Paper›PMID 41888933›Full record

ReviewOrphanet journal of rare diseases2026

Clinical and genetic characteristics of and diagnostic insights on KBG syndrome in Chinese patients: a retrospective study and literature review.

Shi-Qi Wang, Sheng-Nan Wu, Hai-Yan Wei, Nan Lv, Li-Fang Song, Dong-Xiao Li, Chang Su, Yong-Xing Chen

Abstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

8 authors.

Shi-Qi WangDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Sheng-Nan WuDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Hai-Yan WeiDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Nan LvZhengzhou Children's Hospital Rehabilitation Center, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Li-Fang SongDepartment of Neurology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Dong-Xiao LiHenan Children's Neurodevelopment Engineering Research Center, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Chang SuDepartment of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China. changsulucky@yahoo.com.
Yong-Xing ChenDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China. cyx75@126.com.ORCID http://orcid.org/0000-0002-2213-0944

Funding

Zhengzhou Science and Technology Beneficiary Program Project 2022KJHM0005
6 · The paper itself

Abstract

backgroundMost published cohorts of individuals with KBG are Caucasian which limits the understanding of the genetic diversity and clinical presentation across ethnicities. Herein, we report Chinese patients with KBGS, summarise their clinical and genetic characteristics, and compare their characteristics with those of non-Chinese patients. We retrospectively analysed the data of 65 Chinese patients, identified 33 previously unreported cases, and compared their data with those of 519 non-Chinese patients.

resultsWe noted the most prevalent features in Chinese patients. Large and/or prominent ears, triangular faces, anteverted nares, synophrys, long philtrum, low hairline, spinal anomalies, and recurrent otitis media differed significantly among ethnicities. Among the 51 patients with the c.1903_1907del variant, there were differences across ethnicities; the c.1903_1907del and non-c.1903_1907del variants differed among Chinese patients. Rare phenotypes were identified in Chinese patients. The incidence of IUGR, polyhydramnios, abnormal renal and brain morphology, abnormal cardiovascular system morphology, preterm birth, and higher NT was higher in all patients. Genetic sequencing revealed 14 unreported variants. Eight patients were treated with recombinant human growth hormone and had increased height without significant adverse effects.

conclusionsOur findings support the consideration of KBGS in the differential diagnosis when specific prenatal features (such as IUGR and polyhydramnios) are present. In such scenarios, referral for genetic counseling to discuss the option of testing for ANKRD11 variants and 16q24.3 microdeletions is a prudent clinical step.Overall, Chinese patients with KBGS appear to tolerate growth hormone treatment, but further studies are needed to confirm its long-term safety and efficacy.

Indexed as

Abnormalities, MultipleBone Diseases, DevelopmentalIntellectual DisabilityTooth AbnormalitiesAdolescentChildChild, PreschoolEast Asian PeopleFaciesFemaleHumansInfantMaleRetrospective Studies16q24.3 deletionANKRD11 variationKBG syndromePerinatalPhenotypic difference

Identifiers

PMID41888933
PMCPMC13682109

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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.