Evidence map›Paper›PMID 26494713›Full record

ArticleBMJ case reports2015

Recurrent episodes of unexplained hypoelectrolytaemia of a rare cause in a young Saudi girl.

Mohsen Suliaman Al-Atawi, Sulaiman Abdullah Al-Queflie, Hamad Abdullah Al-Sadoon

Abstract readCase Reports
In one paragraph

Article in BMJ case reports, 2015. 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

3 authors.

Mohsen Suliaman Al-AtawiDepartment of Pediatric, King Abdulaziz Medical City, Riyadh, Central Region, Saudi Arabia.
Sulaiman Abdullah Al-QueflieDepartment of Pediatric, King Abdulaziz Medical City, Riyadh, Central Region, Saudi Arabia.
Hamad Abdullah Al-SadoonDepartment of Pediatric, King Abdulaziz Medical City, Riyadh, Central Region, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a case of a 36-month-old Saudi girl who presented with recurrent episodes of unexplained hypoelectrolytaemia. Her cystic fibrosis CFTR (Cystic Fibrosis Transmembrane conductance Regulator) full gene sequence confirmed that she was homozygous for D579G mutation.

Indexed as

Child, PreschoolCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleHomozygoteHumansMutationRecurrenceSaudi ArabiaWater-Electrolyte ImbalanceCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID26494713
PMCPMC4620217

What OpenQuestion holds

Textmetadata
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.