Focal segmental glomerulosclerosis (FSGS) is a disease where scar tissue forms on areas of the kidneys that filter waste from the blood, which is called glomeruli. FSGS is one of the causes of nephrotic syndrome.
Kidneys are made up of about a million tiny filters called glomeruli. Glomeruli filter blood, taking out the water-like the substance that becomes urine and leaving in protein. When glomeruli become damaged or scarred, proteins begin leaking into the urine.
There are three types of FSGS:
Genetic (or familial) FSGS
What are the symptoms of FSGS?
Protein in urine
Edema (swelling around eyes, hands, feet, and abdomen)
Low blood albumin levels
High levels of creatinine
High blood pressure
What causes FSGS?
The cause depends on the type of FSGS:
Primary FSGS – idiopathic, i.e. has no known cause
Secondary FSGS – caused by:
Kidney defects from birth (dysplasia)
Urine backing up into kidneys (kidney reflux)
Obstructive Sleep Apnea
Viruses and blood disorders
Autoimmune disorders (such as lupus and HSP)
Genetic (or familial) FSGS – caused by genetic mutations.
How is FSGS diagnosed?
Medical exams to help reach a diagnosis include:
Blood tests to check cholesterol level
What are the treatments for FSGS?
A steroid called prednisone or prednisolone to mitigate proteinuria
Medications that suppress the immune system
Diuretics and low salt diet help to control edema
Medication that blocks a hormone system called the renin angiotensin system to control blood pressure or lower urine protein
We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!
We’ve heard your feedback. Now, by creating a login below, you can customize your homepage to the rare conditions that are most important to you. You can also share your rare story directly through the site, so being part of our community is easier than ever!