https://cyclosporinainhibitor.....com/protective-resul
Two patients with PTC and a validated heterozygous MEN1 gene mutation are the subject of these clinical case presentations. The complexity of morphological PTC diagnosis is evident in these cases, reflecting the diverse clinical presentations in individuals with the MEN1 mutation. This emphasizes the importance of early screening efforts to detect additional components of MEN1 syndrome and identify related gene mutations in the family. Alt
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