Multifactorial Origin of Exertional Rhabdomyolysis, Recurrent Hematuria, and Episodic Pain in a Service Member with Sickle Cell Trait
Individuals with Sickle Cell Trait (SCT), generally considered a benign carrier state of hemoglobin S (HbAS), are thought to be at risk for exertional rhabdomyolysis and hematuria, conditions that can also be caused by various other acquired and inherited factors. We report an SCT positive service m...
Saved in:
Main Authors: | Nyamkhishig Sambuughin, Mingqiang Ren, John F. Capacchione, Ognoon Mungunsukh, Kevin Chuang, Iren Horkayne-Szakaly, Francis G. O’Connor, Patricia A. Deuster |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2018-01-01
|
Series: | Case Reports in Genetics |
Online Access: | http://dx.doi.org/10.1155/2018/6898546 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Review on Hematuria in Children
by: Sarel Halachmi, et al.
Published: (2006-01-01) -
Drug discovery: a multifactorial ecosystem
by: Fernando Albericio
Published: (2023-01-01) -
A telemedicine triage model for infusion center–based management of adult sickle cell pain episodes
by: John Bliamptis, et al.
Published: (2025-02-01) -
Multifactorial QT Interval Prolongation and Takotsubo Cardiomyopathy
by: Michael Gysel, et al.
Published: (2014-01-01) -
Nutcracker Syndrome: A Rare Cause of Hematuria
by: Emmanuel C. Gorospe, et al.
Published: (2006-01-01)