Familial Hemophagocytic Lymphohistiocytosis Type 3 with Demyelinating CNS Disease

J Gordon Millichap

doi:10.15844/pedneurbriefs-23-2-5

Familial Hemophagocytic Lymphohistiocytosis Type 3 with Demyelinating CNS Disease

Pediatric Neurology Briefs

Volume 23 (2009): Issue 2

By: J Gordon Millichap

Open Access

|Feb 2009

Abstract

A case of familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting in a 3-year-old boy with fulminant demyelinating neurological disease is reported by researchers at Kravis Children’s Hospital at Mount Sinai Medical Center, New York.

References

Weisfeld-Adams JD Frank Y Havalad V Hojsak JM Posada R Kaicker SM Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease Childs Nerv Syst 2009 Feb 25 2 153 9 10.1007/s00381-008-0744-z 19023578
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-23-2-5 | Journal eISSN: 2166-6482

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Language: English

Page range: 12 - 12

Published on: Feb 1, 2009

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Familial Hemophagocytic Lymphohistiocytosis,

Neurological Symptoms,

Perivascular White

© 2009 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 23 (2009): Issue 2