Rare Association between Two Genetic Conditions: Turner Syndrome and Neurofibromatosis Type 1.

R El Qadiry, K Danaoui, H Nassih, A Bourrahouat, I Ait Sab

Abstract readCase Reports

In one paragraph

Article in Case reports in endocrinology, 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

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.

CONCURRENT OCCURRENCE OF NEUROFIBROMATOSIS TYPE 1 AND TURNER SYNDROME: A PEDIATRIC CASE REPORT WITH COMPREHENSIVE LITERATURE REVIEW.Acta endocrinologica (Bucharest, Romania : 2005)
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.

R El QadiryPediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.ORCID https://orcid.org/0000-0002-3984-2307

K DanaouiPediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.

H NassihPediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.ORCID https://orcid.org/0000-0002-7127-4135

A BourrahouatPediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.

I Ait SabPediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Turner's syndrome (TS) is a sex chromosome disorder due to loss of either all or part of the X chromosome, in some or all the cells of the body. Neurofibromatosis type 1 (NF-1) is a multisystemic genetic disorder that is only rarely observed in association with Turner syndrome. Only six cases of Turner syndrome associated with NF-1 have been reported in the literature. In this study, we report the first case with TS and NF-1 in a Moroccan child.

Identifiers

PMID35463623

DOI10.1155/2022/6116603

PMCPMC9033354

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.