Evidence map›Paper›PMID 31230109›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2019

GAPO syndrome with craniosynostosis and intracranial hypertension.

Mehdi Golpayegani, Farhad Salari, Zohreh Habibi, Negin Naderian, Farideh Nejat

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2019. 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, top 95% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Management of secondary intracranial hypertension in untreated craniosynostosis: a case series and literature review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    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 1 country.

Mehdi GolpayeganiDepartment of Neurosurgery, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Farhad SalariDepartment of Neurosurgery, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Zohreh HabibiDepartment of Neurosurgery, Children's Medical Center, Tehran University of Medical Sciences, Gharib street, Tehran, 1419733151, Iran.
Negin NaderianDepartment of Neurosurgery, Children's Medical Center, Tehran University of Medical Sciences, Gharib street, Tehran, 1419733151, Iran.
Farideh NejatDepartment of Neurosurgery, Children's Medical Center, Tehran University of Medical Sciences, Gharib street, Tehran, 1419733151, Iran. nejat@sina.tums.ac.ir.
Shahid Beheshti University of Medical Sciences · IRTehran University of Medical Sciences · IRChildren's Medical Center · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGAPO (growth retardation, alopecia, pseudoanodontia, and optic atrophy) as a rare genetic disorder includes growth retardation, alopecia, pseudoanodontia, and optic atrophy. It was reported to be associated with craniosynostosis and intracranial hypertension. CASE REPORT: A patient with such a rare disorder associated with multisuture craniosynostosis and headache is presented. Surgery has been done due to intracranial hypertension.

conclusionsAbnormal intraoperative findings including sever pericranium and dural adhesions and extraordinary bleeding related to this syndrome are described.

Indexed as

AlopeciaAnodontiaChild, PreschoolCraniosynostosesCraniotomyFemaleGrowth DisordersHumansIntracranial HypertensionOptic Atrophies, HereditaryTreatment OutcomeCraniosynostosisDuraGAPO syndromePericranium

Identifiers

PMID31230109
OpenAlexW2951307342

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.