Format

Send to:

Choose Destination

Links from PubMed

Items: 3

1.

NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO

MedGen UID:
865338
Concept ID:
C4016901
Finding
2.

Nephrotic Syndrome, Idiopathic

MedGen UID:
501252
Concept ID:
C3496337
Disease or Syndrome
3.

Nephrotic syndrome, idiopathic, steroid-resistant

Steroid-resistant nephrotic syndrome type 2 is an autosomal recessive disorder characterized clinically by childhood onset of proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Kidney biopsies show nonspecific histologic changes such as minimal change, focal segmental glomerulosclerosis (FSGS), and diffuse mesangial proliferation. The disorder is resistant to steroid treatment and progresses to end-stage renal failure in the first or second decades (summary by Fuchshuber et al., 1996). Some patients show later onset of the disorder (Tsukaguchi et al., 2002). For a general phenotypic description and a discussion of genetic heterogeneity of nephrotic syndrome and FSGS, see NPHS1 (256300). [from OMIM]

MedGen UID:
358380
Concept ID:
C1868672
Disease or Syndrome
Format

Send to:

Choose Destination

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...