Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy
Type 1 pseudohypoaldosteronism (PHA1) is a salt wasting syndrome caused by renal resistance to aldosterone. Primary renal PHA1 or autosomal dominant PHA1 is caused by mutations in mineralocorticoids receptor gene (NR3C2), while secondary PHA1 is frequently associated with urinary tract infection (UT...
Saved in:
| Main Authors: | Sasigarn A. Bowden, Corin Cozzi, Scott E. Hickey, Devon Lamb Thrush, Caroline Astbury, Sushma Nuthakki |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2013-01-01
|
| Series: | Case Reports in Endocrinology |
| Online Access: | http://dx.doi.org/10.1155/2013/524647 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Secondary pseudohypoaldosteronism caused by urinary tract infection associated with urinary tract anomalies: case reports
by: Meral Torun-Bayram, et al.
Published: (2012-02-01) -
Secondary pseudohypoaldosteronism caused by urinary tract infection associated with urinary tract abnormalities: case reports
by: Onur Sakallıoğlu
Published: (2012-12-01) -
Optimizing the lithotripsy timing after drainage of the upper urinary tract in patients with urolithiasis and obstructive uropathy
by: A. I. Khotko, et al.
Published: (2021-10-01) -
A case report on pseudohypoaldosteronism with a pathogenic mutation of CA12 causes autosomal recessive isolated hyperchlorhidrosis disorder
by: Yousef A. Alanazi
Published: (2025-06-01) -
RADIONUCLIDE EVALUATION OF URETERAL URINARY TRANSIT IN CHILDREN WITH OBSTRUCTIVE UROPATHIES
by: A. G. Burkin, et al.
Published: (2012-04-01)