1型神经纤维瘤病的生殖问题:最新进展

F. Pepe, Paolo Santoro, M. Monteleone, G. Insalaco
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引用次数: 0

摘要

RASMEK-ERK通路的成分或调节因子发生种系突变导致的一系列临床疾病。它们包括1型神经纤维瘤病(NF1)、Costello综合征、Noonan综合征、多发性扁豆精的Noonan综合症、Legis综合征、心面部皮肤综合征、毛细血管畸形动静脉综合征、牙龈纤维瘤病和自身免疫性淋巴增生综合征[1]。这些综合征总共影响1∶1000名新生儿[2]。每种综合征都有不同的临床方面,尽管有些特征是重叠的,需要分子诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reproductive Issues in Neurofibromatosis Type 1: An Update
RASopathies are a clinical spectrum of diseases due to germline mutation in components or regulators of the RASMEK-ERK pathways. They include neurofibromatosis type 1 (NF1), Costello syndrome, Noonan syndrome, Noonan syndrome with multiple lentigines, Legis syndrome, cardio faciocutaneous syndrome, capillary malformationarteriovenous syndrome, gingival fibromatosis and autoimmune lymphoproliferative syndrome [1]. Altogether these syndrome affects 1:1,000 newborns [2]. Each syndrome has distinct clinical aspects, although some characteristics are overlapping needing molecular diagnosis.
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