Evidence map›Paper›PMID 37529132›Full record

ArticleClinical case reports2023

Report of two cases of Schaaf-Yang syndrome: Same genotype and different phenotype.

Ana Maria Rodriguez, Katherine Schain, Parul Jayakar, Meredith S Wright, Shimul Chowdhury, Daria Salyakina

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. MAGEL2 (patho-)physiology and Schaaf-Yang syndrome.Developmental medicine and child neurology · 2025
    Review
  3. 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.

Ana Maria RodriguezDivision of Genetics and Metabolism Nicklaus Children's Hospital Pediatric Specialists Miami Florida USA.ORCID https://orcid.org/0000-0002-9227-8979
Katherine SchainDivision of Genetics and Metabolism Nicklaus Children's Hospital Pediatric Specialists Miami Florida USA.
Parul JayakarDivision of Genetics and Metabolism Nicklaus Children's Hospital Pediatric Specialists Miami Florida USA.
Meredith S WrightRady Children's Institute for Genomic Medicine San Diego California USA.
Shimul ChowdhuryRady Children's Institute for Genomic Medicine San Diego California USA.
Daria SalyakinaPersonalized Medicine & Health Outcomes Research, Nicklaus Children's Hospital Pediatric Specialists Miami Florida USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report two, genotypically identical but phenotypically distinct cases of Schaaf-Yang syndrome and propose the early use of Genome Sequencing in patients with nonspecific presentations to facilitate the early diagnosis of children with rare genetic diseases and improve overall health care outcomes.

Indexed as

ICUMAGEL2phenotype–genotype associationrapid whole genome sequencing

Identifiers

PMID37529132
PMCPMC10387585

What OpenQuestion holds

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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.