Evidence map›Paper›PMID 36728277›Full record

ArticleJournal of clinical research in pediatric endocrinology2024

Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the

Basma Haris, Idris Mohammed, Umm-Kulthum Ismail Umlai, Diksha Shirodkar, Khalid Hussain

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2024. 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, top 98% 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

3 citing papers in PubMed, 0 citations in OpenAlex.

  1. Article
  2. Analysis of Genetic Factors in a Family With Short Stature.Molecular genetics & genomic medicine · 2026
    Article
  3. [Growth plate regulation and short stature: mechanistic insights and therapeutic advances].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    Review
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 3 institutions in 2 countries.

Basma HarisSidra Medicine, Department of Pediatric Endocrinology, Doha, QatarORCID 0000-0003-0486-8010
Idris MohammedSidra Medicine, Department of Pediatric Endocrinology, Doha, QatarORCID 0000-0002-8983-0929
Umm-Kulthum Ismail UmlaiHamad Bin Khalifa University, College of Health and Life Sciences, Doha, QatarORCID 0000-0002-4150-5027
Diksha ShirodkarYenepoya Medical College and Hospital, Department of Paediatrics, Mangalore, Karnataka, IndiaORCID 0000-0002-5958-9281
Khalid HussainSidra Medicine, Department of Pediatric Endocrinology, Doha, QatarORCID 0000-0002-5480-7112
Hamad bin Khalifa University · QAQatar Airways (Qatar) · QAYenepoya University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growth disorders resulting in extreme short stature (ESS) are often a result of deficiency in growth hormone (GH) released from the pituitary gland or a defective GH releasing receptor. Genetic defects in the

Indexed as

HomozygoteHuman Growth HormoneChild, PreschoolDwarfism, PituitaryGrowth DisordersHumansIndiaMaleSequence DeletionHuman Growth Hormonefamilial short statureGH gene deletionshort stature

Identifiers

PMID36728277
PMCPMC11590716
OpenAlexW4318913344

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.