Hemolytic-uremic syndrome risk factors: Difference between revisions
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==Risk Factors== | ==Risk Factors== | ||
The most potent risk factor in the development of HUS is etiology advanced and Clinical associations . Other risk factors include [etiology unknown]. | |||
'''etiology advance ''' | |||
*Infection induced | |||
#Shiga and verocytotoxin (shiga-like toxin)-producing bacteria;enterohemorrhagic Escherichia coli, Shigella dysenteriaen type 1,Citrobacter | |||
#Streptococcus pneumoniae, neuraminidase, and T-antigen exposure | |||
*Disorders of complement regulation | |||
# Genetic disorders of complement regulation | |||
# Acquired disorders of complement regulation, for example anti-FH antibody | |||
*von Willebrand proteinase, ADAMTS13 deficiency | |||
# Genetic disorders of ADAMTS13 | |||
* | #Acquired von Willebrand proteinase deficiency; autoimmune, drug induced | ||
*Defective cobalamine metabolism | |||
and Qinine induced . | |||
clinical associations | |||
#HIV | |||
#Malignancy, cancer chemotherapy and ionizing radiation | |||
#Calcineurin inhibitors and transplantation | |||
#Pregnancy, HELLP syndrome and oral contraceptive pill | |||
#Systemic lupus erythematosis and antiphospholipid antibody syndrome | |||
#Glomerulopathy | |||
#Familial, not included in part 1 | |||
#Unclassified | |||
==References== | ==References== |
Revision as of 19:55, 23 July 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
There are no established risk factors for [disease name].
OR
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
Risk Factors
The most potent risk factor in the development of HUS is etiology advanced and Clinical associations . Other risk factors include [etiology unknown].
etiology advance
- Infection induced
- Shiga and verocytotoxin (shiga-like toxin)-producing bacteria;enterohemorrhagic Escherichia coli, Shigella dysenteriaen type 1,Citrobacter
- Streptococcus pneumoniae, neuraminidase, and T-antigen exposure
- Disorders of complement regulation
- Genetic disorders of complement regulation
- Acquired disorders of complement regulation, for example anti-FH antibody
- von Willebrand proteinase, ADAMTS13 deficiency
- Genetic disorders of ADAMTS13
- Acquired von Willebrand proteinase deficiency; autoimmune, drug induced
- Defective cobalamine metabolism
and Qinine induced .
clinical associations
- HIV
- Malignancy, cancer chemotherapy and ionizing radiation
- Calcineurin inhibitors and transplantation
- Pregnancy, HELLP syndrome and oral contraceptive pill
- Systemic lupus erythematosis and antiphospholipid antibody syndrome
- Glomerulopathy
- Familial, not included in part 1
- Unclassified