Back to search

Article

NPHS2 Mutations in Familial Steroid Resistant Nephrotic Syndrome in Gaza

2017-01-01

Abstract excerpt

Background: Nephrotic syndrome (NS) is characterized by edema, massive proteinuria, hypoalbuminemia, hyperlipidemia, and may progress to end stage renal disease. Based on the response to steroid therapy, NS is categorized as steroid-sensitive or steroid-resistant (SRNS). SRNS is inherited as an autosomal recessive disorder with NPHS2 being the most frequently mutated gene. NPHS2 encodes the glomerular protein podo...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
23f3aeac-24b4-5b7f-9411-cf14445e3d12
DOI
10.25141/2577-0152-2017-1.0027
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
NPHS2 Mutations in Familial Steroid Resistant Nephrotic Syndrome in GazaDOI 10.25141/2577-0152-2017-1.0027
Select a neighboring publication to make it the new centre.