Results 141 to 150 of about 2,952,556 (266)
First report of hyperphosphatemic familial tumoral calcinosis due to homozygous GALNT3 mutation in a 16-year-old boy [PDF]
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare disorder HFTC is caused by a loss of function in fibroblast growth factor 23 (FGF23), leading to increased phosphate levels in the body and calcium deposition.
Gupta, Sushil +2 more
core +2 more sources
Tumoral calcinosis, a diagnostic dilemma: a case report
Javed Altaf +4 more
openalex +2 more sources
Genetic diseases resulting from disordered FGF23/klotho biology [PDF]
Econs, Michael J.
core +1 more source
AB0003 A galnt3 gene mutation in two sibs with chronic recurrent multifocal osteomyelitis associated with hyperphosphatemic familial tumoral calcinosis [PDF]
D. El Dessouki +4 more
openalex +1 more source
Calcinosis tumoral urémica. Reporte de caso
Introducción. La calcinosis tumoral (CT) es una afección rara caracterizada por el depósito de sales de calcio en los tejidos blandos periarticulares. Cuando ocurre en presencia de enfermedad renal crónica (ERC) se conoce como CT urémica.
Cristian Alexis Tarazona-Guerrero +4 more
doaj +1 more source
Tumoral Calcinosis at Unusual Site: Diagnosis on Fine Needle Aspiration Cytology
Shilpa Pateria +3 more
openalex +1 more source
An unusual laryngeal mass: primary tumoral calcinosis of the larynx in a child
Background: Tumoral calcinosis (TC) is a rare, benign calcium hydroxyapatite deposition typically affecting periarticular tissue of large joints, which may occur sporadically or in association with hyperphosphatemia.
Miles J. Klimara +3 more
doaj +1 more source

