Evidence map›Paper›PMID 35865771›Full record

ArticleClinical case reports2022

A case report of McCune-Albright syndrome with hepatic manifestations.

Mohammad Haddadi, Elahe Lal Kheirkhah, Mojgan Ansari, Samieh Ahmadzade, Zeinab Taraz, Saeid Yazdi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2022. 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
0.5field-weighted citation impact, top 34% 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, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 5 institutions in 1 country.

Mohammad HaddadiDepartment of Nursing Tabas Branch Islamic Azad University Tabas Iran.
Elahe Lal KheirkhahDepartment of Nursing Esfarayen University of Medical Sciences Esfarayen Iran.ORCID https://orcid.org/0000-0001-5934-4690
Mojgan AnsariDepartment of Nursing, Nursing & Midwifery School Sabzevar University of Medical Sciences Sabzevar Iran.
Samieh AhmadzadeImam Khomeini Hospital Esfarayen Faculty of Medical Sciences Esfarayen Iran.
Zeinab TarazPayambar Azam Hospital Kerman Faculty of Medical Sciences Kerman Iran.
Saeid YazdiImam Khomeini Hospital Esfarayen Faculty of Medical Sciences Esfarayen Iran.
Imam Khomeini Hospital · IREsfarayen University of Technology · IRIslamic Azad University, Tehran · IRKerman University of Medical Sciences · IRSabzevar University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

McCune-Albright syndrome is a non-hereditary disease characterized by café-au-lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture. During the follow-up, liver function tests were abnormal. Considering the clinical and paraclinical findings, the patient was diagnosed with McCune-Albright syndrome.

Indexed as

bone fibrous dysplasiaGNAS gene mutationMcCune–Albright syndromeneonatal cholestasis

Identifiers

PMID35865771
PMCPMC9295684
OpenAlexW4286255289

What Socratic 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 Socratic graph.