Noonan syndrome with RAF1 gene mutations in a newborn with cerebral haemorrhage

Noonan syndrome with RAF1 gene mutations in a newborn with cerebral haemorrhage

Abstract Background Noonan syndrome is an autosomal dominant genetic disorder that can occur in men and women and has a sporadic or family history. NS can lead to abnormal bleeding, but cerebral haemorrhage is rare. This is the first case of cerebral haemorrhage with a RAF1 gene mutation that origin...

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Bibliographic Details
Main Authors: Junwei Lan, Tianbao Zeng, Sheng Liu, Juhong Lan, Lijun Qian
Format: Article
Language:English
Published: BMC 2022-08-01
Series:European Journal of Medical Research
Subjects:
Noonan syndrome
RAF1, cerebral haemorrhage
Newborn
46, X, del (Y) (q12)
Online Access:https://doi.org/10.1186/s40001-022-00772-2

Internet

https://doi.org/10.1186/s40001-022-00772-2

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