Progressive polyradiculoneuropathy due to intraneural oxalate deposition in type 1 primary hyperoxaluria

ABSTRACT Introduction: A 24‐year‐old man with primary hyperoxaluria type 1 (PH1) presented with a rapidly progressive axonal and demyelinating sensorimotor polyradiculoneuropathy shortly after the onset of end‐stage renal disease. His plasma oxalate level was markedly elevated at 107 µmol/L (normal...

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Bibliographic Details
Published in:Muscle & nerve 2015-03, Vol.51 (3), p.449-454
Main Authors: Berini, Sarah E., Tracy, Jennifer A., Engelstad, Janean K., Lorenz, Elizabeth C., Milliner, Dawn S., Dyck, Peter J.
Format: Article
Language:English
Subjects:
Calcium Oxalate - metabolism
crystalline neuropathy
Disease Progression
Humans
Hyperoxaluria, Primary - complications
Hyperoxaluria, Primary - diagnosis
Hyperoxaluria, Primary - metabolism
Male
nerve pathology
peripheral neuropathy
Polyradiculoneuropathy - diagnosis
Polyradiculoneuropathy - etiology
Polyradiculoneuropathy - metabolism
primary hyperoxaluria type 1
renal failure
Sural Nerve - metabolism
Sural Nerve - pathology
Young Adult
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Summary:ABSTRACT Introduction: A 24‐year‐old man with primary hyperoxaluria type 1 (PH1) presented with a rapidly progressive axonal and demyelinating sensorimotor polyradiculoneuropathy shortly after the onset of end‐stage renal disease. His plasma oxalate level was markedly elevated at 107 µmol/L (normal
ISSN:0148-639X
1097-4598
DOI:10.1002/mus.24495