Evidence map›Paper›PMID 32508745›Full record

ReviewFrontiers in endocrinology2020

Genetic Evaluation of Patients With Delayed Puberty and Congenital Hypogonadotropic Hypogonadism: Is it Worthy of Consideration?

Adalgisa Festa, Giuseppina Rosaria Umano, Emanuele Miraglia Del Giudice, Anna Grandone

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Adalgisa FestaDepartment of Woman, Child, General and Specialized Surgery, University of Campania L. Vanvitelli, Naples, Italy.
Giuseppina Rosaria UmanoDepartment of Woman, Child, General and Specialized Surgery, University of Campania L. Vanvitelli, Naples, Italy.
Emanuele Miraglia Del GiudiceDepartment of Woman, Child, General and Specialized Surgery, University of Campania L. Vanvitelli, Naples, Italy.
Anna GrandoneDepartment of Woman, Child, General and Specialized Surgery, University of Campania L. Vanvitelli, Naples, Italy.
University of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Delayed puberty is a common reason of pediatric endocrinological consultation. It is often a self-limited (or constitutional) condition with a strong familial basis. The type of inheritance is variable but most commonly autosomal dominant. Despite this strong genetic determinant, mutations in genes implicated in the regulation of hypothalamic-pituitary-gonadal axis have rarely been identified in cases of self-limited delayed puberty and often in relatives of patients with congenital hypogonadotropic hypogonadism (i.e.,

Indexed as

Genetic MarkersChildEvaluation Studies as TopicHumansHypogonadismPuberty, DelayedGenetic Markersgeneticshypogonadal hypogonadismnext-generation sequencingpediatricspuberty

Identifiers

PMID32508745
PMCPMC7248176
OpenAlexW3028280152

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.