Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Hyperphosphatemic pseudotumoral calcinosis due to FGF23 mutation with secondary amyloidosis].

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia - 29 Aug 2022

Sottini Laura, Veniero Patrizia, De Gaetano Andrea, Olivi Laura, Brunori Giuliano

Abstract excerpt

A 44 years old man was admitted for nephrotic syndrome and rapidly progressive renal failure. Two firm, tumour-like masses were localized around the left shoulder and the right hip joint. Since the age of 8 years old, the patient had a history of metastatic calcification of the soft tissues suggesting hyperphosphatemic pseudotumoral calcinosis. Despite treatment for a long time with phosphate binders the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyloidosis
Share to Calcinosis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Fibroblast Growth Factors

Share to Nephrotic Syndrome

Share to Phosphates

Share to Renal Insufficiency

Share to Serum Amyloid A Protein

Source

Identifiers

PMID: 36073335

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

[Hyperphosphatemic pseudotumoral calcinosis due to FGF23 mutation with secondary amyloidosis].PMID 36073335Read ↗

Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature.Semantic proximity Read ↗

[Familial tumoral calcinosis with hyperphosphatemia is heterogeneous and associated with mutations in GALNT3 or FGF-23].Semantic proximity Read ↗

Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation.Semantic proximity Read ↗

Familial tumoral calcinosis caused by a novel FGF23 mutation: response to induction of tubular renal acidosis with acetazolamide and the non-calcium phosphate binder sevelamer.Semantic proximity Read ↗

A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcificationSemantic proximity Read ↗

[Familial tumoral calcinosis in three patients in the same family].Semantic proximity Read ↗

A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis.Semantic proximity Read ↗

[Pseudoidiopathic hypoparathyroidism].Semantic proximity Read ↗

A novel recessive mutation of fibroblast growth factor-23 in tumoral calcinosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.