Evidence map›Paper›PMID 39493154›Full record

ArticleCureus2024

Report of DeSanto-Shinawi Syndrome in Three Boys With Two Novel Variants in the WAC Gene and Expansion of the Phenotype.

Zuhair Rahbeeni, Nabilah Alwadani, Maryam Al-Shehhi, Eisa A Faqeih, Sarar Mohamed

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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.

Zuhair RahbeeniGenetics, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
Nabilah AlwadaniGenetics, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
Maryam Al-ShehhiGenetics, Sheikh Khalifa Medical City, Abu Dhabi, ARE.
Eisa A FaqeihGenetics, King Fahad Medical City, Riyadh, SAU.
Sarar MohamedGenetics, Prince Sultan Military Medical City, Riyadh, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Desanto-Shinawi syndrome (DESSHS) is a rare autosomal dominant disorder caused by a loss of function variant or deletion of the WAC gene. DESSHS is characterized by dysmorphic features and global developmental delay. In this report, we discuss three boys with DESSHS. These three patients exhibited the characteristic facial dysmorphism, intellectual disability, and behavioral problems associated with DESSHS. In addition, the patients presented with features not previously associated with DESSHS, including choanal atresia, flat feet, hypospadias, caudothalamic groove, and periventricular leukomalacia. Two of our patients had novel sequence variants (de-novo) in the WAC gene, specifically c.921del (p. E307Dfs*24) and c.479delC (p. Pro160fs*32). The third variant was a 9,389 kbp deletion on chromosome 10p12.31p11.22, resulting in the deletion of 74 genes, including the WAC gene. This report highlights manifestations not previously reported with DESSHS and may expand the understanding of this rare disorder. Furthermore, two new variants were detected in our patients.

Indexed as

desanto-shinawi syndromeexpansionnovelphenotypevariantwac gene

Identifiers

PMID39493154
PMCPMC11531785

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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.