A Familial Case of a Whole Germline CDC73 Deletion Discordant for Primary Hyperparathyroidism

一例家族性原发性甲状旁腺功能亢进症患者,该病与全生殖系 CDC73 基因缺失不一致

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作者:Naomi Hatabu, Naho Katori, Takeshi Sato, Naonori Maeda, Eri Suzuki, Osamu Komiyama, Hidemitsu Tsutsui, Toshitaka Nagao, Hana Nakauchi-Takahashi, Tatsuo Matsunaga, Tomohiro Ishii, Tomonobu Hasegawa, Kazuki Yamazawa

Conclusions

These data clearly demonstrate the Knudson two-hit theory from a molecular viewpoint. Phenotypic variability and incomplete penetrance of CDC73-related disorders, even if caused by a gross deletion, should be noted in a clinical setting.

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