Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis
Abstract Background Familial hemophagocytic lymphohistiocytosis (FLH) is an autosomal recessive disorder of immune regulation that leads to a hyperinflammatory syndrome. Fetal onset FHL is extremely rare and is considered to be the most severe form of FHL. Case We report a preterm case of FHL that p...
Saved in:
Main Authors: | Sota Iwatani (Author), Kazuya Uemura (Author), Masami Mizobuchi (Author), Seiji Yoshimoto (Author), Keiichiro Kawasaki (Author), Yoshiyuki Kosaka (Author), Masayuki Hori (Author), Takahiro Yasumi (Author), Hideto Nakao (Author) |
---|---|
Format: | Book |
Published: |
Thieme Medical Publishers, Inc.,
2015-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Successful Management of an Extremely Premature Infant with Congenital Candidiasis
by: Sota Iwatani, et al.
Published: (2014) -
Etiology and Outcome of Hydrops Fetalis
by: Jia-Yuh Chen
Published: (2014) -
Non-immune hydrops fetalis
by: Murat Yurdakök
Published: (2014) -
HEMOPHAGOCYTAL LYMPHOHISTIOCYTOSIS
by: M.A. Maschan, et al.
Published: (2009) -
HEMOPHAGOCYTAL LYMPHOHISTIOCYTOSIS
by: M.A. Maschan, et al.
Published: (2009)