Evidence map›Paper›PMID 34327088›Full record

ArticleCureus2021

An Extremely Rare Case of Birk-Barel Syndrome With Severe Central Apneas.

Michael A Ramirez-Arenalde, Wilmarie J Bruckman-Blanco, Abymael Frontanes-Heredia, Sherry L Santiago-Castro, Wilfredo De Jesús-Rojas

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 5 institutions in 1 country.

Michael A Ramirez-ArenaldeInternal Medicine, Ponce Health Sciences University, Ponce, PRI.
Wilmarie J Bruckman-BlancoPediatrics, Centro Médico Menonita de Cayey, Cayey, PRI.
Abymael Frontanes-HerediaPediatrics, Centro Médico Menonita de Cayey, Cayey, PRI.
Sherry L Santiago-CastroPediatrics, Universidad Central del Caribe School of Medicine, Bayamón, PRI.
Wilfredo De Jesús-RojasPediatrics, Ponce Health Sciences University, Ponce, PRI.
Central University of the Caribbean · PRPonce Health Sciences University · PRSan Juan Bautista School of Medicine · PRUniversity of Puerto Rico at Cayey · PRUniversity of Puerto Rico, Medical Sciences Campus · PR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Birk-Barel syndrome, alternatively known as KCNK9 imprinting syndrome, is caused by a missense mutation in the potassium two pore domain channel subfamily K member 9 (KCNK9) gene on chromosome 8q24.3. This syndrome demonstrates dominant inheritance and is imprinted with paternal silencing, where the paternally inherited allele is silenced, and the maternally inherited allele is active. Congenital hypotonia, palatal abnormalities, intellectual disability, severe feeding difficulties, and dysmorphic facial features characterize this sporadic genetic syndrome. To date, there are approximately 21 molecularly diagnosed individuals worldwide described in the literature. We describe the first known case of Puerto Rican ethnicity, a 16-month-old female born prematurely at 36-weeks with Birk-Barel syndrome, confirmed with whole-exome sequencing, and her response to non-invasive ventilation as a treatment for her sleep breathing disorder.

Indexed as

birk-barel syndromecentral apneashypotoniaimprintingintellectual disabilitykcnk9maternal inheritancenon invasive ventilationpuerto ricotask3

Identifiers

PMID34327088
PMCPMC8301725
OpenAlexW3174850924

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.