Abstract Aim Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare endocrine disorder caused by autosomal recessive variants in GALNT3, FGF23, and KL leading to progressive calcification of soft tissues and subsequent clinical effects. The aim of this was to study the cause of HFTC in an Iranian family. Patients and methods Four generations...
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Journal Name: Journal of Pediatric Endocrinology and MetabolismIssue: Ahead of print
Journal Name: Journal of Pediatric Endocrinology and MetabolismIssue: Ahead of print
Journal Name: Journal of Pediatric Endocrinology and MetabolismIssue: Ahead of print
Mark above section as read
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