Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency

Neuropediatrics. 2017 Dec;48(6):477-481. doi: 10.1055/s-0037-1604483. Epub 2017 Aug 11.

Authors

Didem Ardicli¹, Ekim Z Taskiran², Can Kosukcu², Cagri Temucin³, Kader K Oguz⁴, Goknur Haliloglu¹, Mehmet Alikasifoglu², Haluk Topaloglu¹

Affiliations

¹ Department of Pediatric Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
² Department of Medical Genetics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
³ Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
⁴ Department of Radiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

PMID: 28800659
DOI: 10.1055/s-0037-1604483

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Anemia, Hemolytic / diagnosis*
Anemia, Hemolytic / genetics*
Anemia, Hemolytic / therapy
Brain / diagnostic imaging
CD59 Antigens / genetics*
Child
Diagnosis, Differential
Female
Guillain-Barre Syndrome / diagnosis*
Guillain-Barre Syndrome / genetics*
Guillain-Barre Syndrome / therapy
Hemoglobinuria / diagnosis*
Hemoglobinuria / genetics*
Hemoglobinuria / therapy
Humans
Recurrence

Substances

CD59 Antigens
CD59 protein, human

Supplementary concepts

CD59 Deficiency