VHL mutation as a cause of three generations familial pheochromocytoma
Abstract Background Pheochromocytoma is a rare disease, and its familial occurrence is quite uncommon. The aim of this paper is to report a three-generation phenotypical expression of a case familial occurrence of pheochromocytoma. Case presentation A 25-year-old female, with a history of adrenalect...
| প্রধান লেখক: | , , , , , , , , |
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| বিন্যাস: | প্রবন্ধ |
| ভাষা: | English |
| প্রকাশিত: |
SpringerOpen
2024-06-01
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| মালা: | Egyptian Journal of Medical Human Genetics |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://doi.org/10.1186/s43042-024-00538-x |