Evidence map›Paper›PMID 41510005›Full record

ArticleKidney medicine2026

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

Geraldine Venessa Qian Le Boh, Hui-Lin Chin, Yao Chun Zhang, Ru Sin Lim

Abstract readCase Reports
In one paragraph

Article in Kidney medicine, 2026. 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.

  1. 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

4 authors.

Geraldine Venessa Qian Le BohDepartment of Renal Medicine, Tan Tock Seng Hospital, Singapore.
Hui-Lin ChinDivision of Genetics and Metabolism, Department of Paediatrics, National University Children's Medical Institute, National University Hospital, Singapore.
Yao Chun ZhangDivision of Genetics and Metabolism, Department of Paediatrics, National University Children's Medical Institute, National University Hospital, Singapore.
Ru Sin LimDepartment of Renal Medicine, Tan Tock Seng Hospital, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

McCune-Albright syndrome (MAS) is a rare systemic genetic condition classically characterized by childhood-onset polyostotic fibrous dysplasia, café-au-lait skin pigmentation, and precocious puberty. Kidney involvement in MAS is infrequently recognized, particularly in low- and middle-income countries where genomic testing may be limited. We presented the first case report of MAS presenting with Fanconi syndrome and progressive kidney failure, which we postulated represents a phenotypic expansion of the renal phenotype associated with MAS, in addition to hyperthyroidism, osteoid osteoma, bone marrow failure secondary to fibrous dysplasia, and congenital ovarian failure. Initial renal biochemical evaluations were suggestive of proximal tubulopathy; however, secondary investigations were inconclusive. Seventeen years after the patient's initial presentation, clinically accredited whole exome sequencing conducted under a national genomic research initiative identified a pathogenic

Indexed as

Fanconi syndromegenomic testingGNAS mutationsG protein-coupled receptorskidney failureMcCune-Albright syndromeproximal tubulopathy

Identifiers

PMID41510005
PMCPMC12774746

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.