| Title: |
Prospective Genetic Screening in Multiple Endocrine Neoplasia Syndromes. |
| Authors: |
Paun, Diana, Tilici, Dana, Paun, Sorin, Mirica, Alexandra |
| Source: |
Children; Aug2024, Vol. 11 Issue 8, p1012, 16p |
| Subject Terms: |
MULTIPLE endocrine neoplasia, DISEASE management, GENE expression, WERMER syndrome, EARLY diagnosis, GENETIC mutation, GENETIC testing, SIPPLE syndrome, MUCOSAL neuroma syndrome, PHENOTYPES, SEQUENCE analysis, GENOTYPES, THYROIDECTOMY |
| Abstract: |
Multiple endocrine neoplasia syndromes are a rare but potentially fatal pathology due to the lack of early diagnosis. We have performed a narrative review of the medical literature, summarizing the main clinical concepts useful in current clinical practice, showing the importance of screening and early diagnosis during childhood. [ABSTRACT FROM AUTHOR] |
|
Copyright of Children is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
| Database: |
Complementary Index |
