The hyperparathyroidism-jaw tumour (HPT-JT) syndrome
The hyperparathyroidsim-jaw tumour (HPT-JT) syndrome is an autosomal dominant disorder characterised by the occurence of parathyroid tumours, which may be carcinomas in approximately 15% of patients, and ossifying fibromes, that usually affect the maxilla and/or mandible. More than 15% of HPT-JT pat...
Hlavní autoři: | Bradley, K, Thakker, R |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2006
|
Podobné jednotky
-
Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal.
Autor: Cavaco, B, a další
Vydáno: (1999) -
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors.
Autor: Newey, P, a další
Vydáno: (2010) -
A two-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report
Autor: Dun Yang, a další
Vydáno: (2022-09-01) -
Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
Autor: Vito Guarnieri, a další
Vydáno: (2017-09-01) -
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.
Autor: Bradley, K, a další
Vydáno: (2005)