Focal segmental glomerulosclerosis
Other Names for this Disease
- Glomerulosclerosis, focal
- Segmental glomerulosclerosis
- Focal sclerosis with hyalinosis
- Familial idiopathic steroid-resistant nephrotic syndrome
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 FSGS may cause non-specific signs and symptoms, including protein in the urine, elevated levels of creatinine, and swelling. In many cases the cause of FSGS can not be determined. Some cases are thought to be associated with congenital kidney defects, urine backing up into the kidneys, obesity, obstructive sleep apnea, sickle cell anemia, or viruses (e.g., HIV). The goal of treatment is to control symptoms and prevent chronic kidney failure. Even with treatment, many people with FSGS progress to kidney failure within 5 to 20 years.Focal segmental glomerulosclerosis (FSGS) is a type of kidney disorder. It is characterized by scar tissue that forms in some of the glomeruli in the kidney.
Last updated: 11/4/2015
- Focal segmental glomerulosclerosis. MedlinePlus. October 21, 2015; http://www.nlm.nih.gov/medlineplus/ency/article/000478.htm. Accessed 11/4/2015.
- Glomerular diseases. National Kidney & Urologic Diseases Information Clearinghouse. April 2, 2014; http://kidney.niddk.nih.gov/kudiseases/pubs/glomerular/. Accessed 11/4/2015.
- Focal segmental glomerulosclerosis (FSGS). UNC Kidney Center Web site. http://unckidneycenter.org/kidney-health-library/glomerular-disease/focal-segmental-glomerulosclerosis-fsgs. Accessed 11/4/2015.
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- Online Mendelian Inheritance in Man (OMIM) lists the subtypes and associated genes for Focal segmental glomerulosclerosis in a table called Phenotypic Series. Each entry in OMIM includes a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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