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...
المؤلفون الرئيسيون: | Bradley, K, Thakker, R |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2006
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مواد مشابهة
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Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal.
حسب: Cavaco, B, وآخرون
منشور في: (1999) -
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors.
حسب: Newey, P, وآخرون
منشور في: (2010) -
A two-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report
حسب: Dun Yang, وآخرون
منشور في: (2022-09-01) -
Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family
حسب: Vito Guarnieri, وآخرون
منشور في: (2017-09-01) -
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.
حسب: Bradley, K, وآخرون
منشور في: (2005)