RASA1-Related Parkes Weber Syndrome in a Neonate
Parkes Weber syndrome is a rare congenital vascular anomaly, related to the RAS p21 protein activator 1 (RASA1) gene. It is characterized by capillary cutaneous malformations, bony and soft tissue hyperplasia, and multiple arteriovenous fistulas throughout the affected upper or lower extremity. Thes...
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Korean Society of Neonatology,
2018-08-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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