Evidence map›Paper›PMID 36045762›Full record

ArticleAnnals of medicine and surgery (2012)2022

A case report of interventricular hemorrhage in William-Beuren syndrome.

Abdullah Alghobaishi, Ahmed Hafez Mousa, Haleema Sami Almonaye, Tasneem Khalid Maghrebi, Abeer Amin, Fawziah Alzaid Al Sharif

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Annals of medicine and surgery (2012), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 90% of its field
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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Heterozygous nonsenseResearch and practice in thrombosis and haemostasis · 2025
    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

6 authors at 2 institutions in 2 countries.

Abdullah AlghobaishiDepartment of Pediatrics, Pediatrics Critical Care Medicine, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
Ahmed Hafez MousaCollege of Medicine and Surgery, Batterjee Medical College, Jeddah, Saudi Arabia.
Haleema Sami AlmonayeCollege of Medicine and Surgery, Batterjee Medical College, Jeddah, Saudi Arabia.
Tasneem Khalid MaghrebiCollege of Medicine and Surgery, Batterjee Medical College, Jeddah, Saudi Arabia.
Abeer AminDepartment of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt.
Fawziah Alzaid Al SharifDepartment of Pediatrics, Saudi German Hospital, Jeddah, Saudi Arabia.
King Fahad Hospital Jeddah · SAKing Fahd Armed Forces Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Williams syndrome (WS) (also as known Williams-Beuren Syndrome) is a neurodevelopmental disorder caused by deletion of chromosomes 7q11.23. WS phenotype is very variable but usually it is associated with a distinctive pattern of cognitive abilities. Case presentation: 9-year-old female patient known case of developmental delay and precocious puberty presented to the emergency department with altered level of consciousness, elevated blood pressure of 230/160 with a provisional diagnosis of hypertensive encephalopathy. Conclusions: In our patient, the strongest indications for establishing the diagnosis included the classic elfin face and multisystemic involvement. Later on genetic analysis confirmed our diagnosis.

Indexed as

7q11.23 deletionGenetic analysisWilliams–beuren-szindrómaWilliams syndrome

Identifiers

PMID36045762
PMCPMC9422350
OpenAlexW4289832725

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.