PTH and FGF23 Exert Interdependent Effects on Renal Phosphate Handling: Evidence from Patients with Hypoparathyroidism and Hyperphosphatemic Familial Tumoral Calcinosis Treated with Synthetic Human PTH 1‐34

2021 ◽  
Author(s):  
Diana Ovejero ◽  
Iris R Hartley ◽  
Luis Fernandez Castro Diaz ◽  
Elizabeth Theng ◽  
Xiaobai Li ◽  
...  
Keyword(s):  
Tumoral Calcinosis ◽  
Hyperphosphatemic Familial Tumoral Calcinosis

scholarly journals Defective O-glycosylation of novel FGF23 mutations in a Chinese family with hyperphosphatemic familial tumoral calcinosis

Bone ◽  
2020 ◽  
Vol 137 ◽  
pp. 115401
Author(s):  
Chang Liu ◽  
Qianqian Pang ◽  
Yan Jiang ◽  
Yu Xia ◽  
Ligang Fang ◽  
...  
Keyword(s):  
Tumoral Calcinosis ◽  
Chinese Family ◽  
Hyperphosphatemic Familial Tumoral Calcinosis

Hyperphosphatemic familial tumoral calcinosis caused by a novel variant in the GALNT3 gene

2020 ◽  
Vol 43 (8) ◽  
pp. 1125-1130
Author(s):  
F. Mahjoubi ◽  
M. Ghadir ◽  
S. Samanian ◽  
I. Heydari ◽  
M. Honardoost
Keyword(s):  
Tumoral Calcinosis ◽  
Novel Variant ◽  
Hyperphosphatemic Familial Tumoral Calcinosis

scholarly journals Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)

2015 ◽  
Vol 120 (6) ◽  
pp. e235-e239 ◽  
Author(s):  
Alexandre R. Vieira ◽  
Moses Lee ◽  
Filippo Vairo ◽  
Julio Cesar Loguercio Leite ◽  
Maria Cristina Munerato ◽  
...  
Keyword(s):  
Autosomal Recessive ◽  
Tumoral Calcinosis ◽  
Hyperphosphatemic Familial Tumoral Calcinosis

scholarly journals Hyperphosphatemic Familial Tumoral Calcinosis Hidden in Plain Sight for 73 Years: A Case Report

2021 ◽  
Vol 2 ◽  
Author(s):  
Alisa E. Lee ◽  
Iris R. Hartley ◽  
Kelly L. Roszko ◽  
Chaim Vanek ◽  
Rachel I. Gafni ◽  
...  
Keyword(s):  
Dental Pulp ◽  
Incidental Findings ◽  
Autosomal Recessive ◽  
Autosomal Recessive Disease ◽  
Mineral Metabolism ◽  
Rare Condition ◽  
Tumoral Calcinosis ◽  
Dental Radiographs ◽  
Hyperphosphatemic Familial Tumoral Calcinosis ◽  
Pulp Calcification

While dental pulp calcifications and root anomalies may be inconsequential incidental findings in dental radiographs, they can, especially in combination, represent a clue, hidden in plain sight, for the diagnosis of hyperphosphatemic familial tumoral calcinosis (HFTC). HFTC is an autosomal recessive disease of mineral metabolism characterized by sometimes massive, painful calcification around large joints, systemic inflammation, dental pulp calcification, and thistle-shaped roots. This paper describes a woman with HFTC who endured not only the symptoms of HFTC for decades, but also the frustration of not knowing the cause. The diagnosis was finally made at the age of 73 years, when the connection between a large right shoulder calcification and hyperphosphatemia was made. The dental findings were likely present on her initial radiographs taken in childhood. Increased awareness of the association between characteristic dental findings and HFTC may allow for earlier diagnosis and interventions to improve the care of patients with this rare condition.

The treatment of Hyperphosphatemic Familial Tumoral Calcinosis

2017 ◽  
Author(s):  
Karine Khatchadourian ◽  
Lou Lawton ◽  
Baxter Willis ◽  
Leanne Ward
Keyword(s):  
Tumoral Calcinosis ◽  
Hyperphosphatemic Familial Tumoral Calcinosis
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