Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates

Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates

Congenital thrombotic thrombocytopenic purpura (TTP) is a rare hereditary disease with a high mortality rate; however, improved patient survival is possible with prompt diagnosis and treatment. The clinical features and mutation sites of a disintegrin and metalloproteinase with thrombospondin motifs...

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Bibliographic Details
Main Authors: Jiali Wang, Li Zhao
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Pediatrics
Subjects:
congenital thrombotic thrombocytopenic purpura
ADAMTS 13
gene mutation
neonates
congenital disease
genetic testing
Online Access:https://www.frontiersin.org/article/10.3389/fped.2020.546248/full

Internet

https://www.frontiersin.org/article/10.3389/fped.2020.546248/full

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