-
Pseudohypoaldosteronism (PHA) is a
condition that
mimics hypoaldosteronism.
Pseudohypoaldosteronism type 1 (PHA1) is
characterized by the body's inability...
- Na+
during the
process of perspiration.
People with the
systemic pseudohypoaldosteronism syndrome who
carry mutations in the ENaC
subunit genes have salty...
- and ARBs, Eplerenone, Spironolactone, Trimethoprim,
Pentamidine Pseudohypoaldosteronism Renal tubular acidosis was
first described in 1935 by Lightwood...
-
Wolfson Medical Center),
identified that a
hereditary disease named pseudohypoaldosteronism (PHA) type I encomp****es two
independent syndromes.
Following this...
- ****ation
Pseudohermaphroditism Pseudohypoaldosteronism type 1
Pseudohypoaldosteronism type 2
Pseudohypoaldosteronism Pseudohypoparathyroidism Pseudomarfanism...
-
encoded by the WNK4 gene.
Missense mutations cause a
genetic form of
pseudohypoaldosteronism type 2, also
called Gordon syndrome. WNK4 is a
member of a serine/threonine...
- (i.e.,
total parenteral nutrition)
Anion gap
Metabolic acidosis Pseudohypoaldosteronism "Hyperchloremic Acidosis:
Practice Essentials, Etiology, Patient...
-
lower blood pressure than non-carriers in the same family. Type II
pseudohypoaldosteronism (PHA2), also
known as Gordon's syndrome, is an
autosomal dominant...
- ****ociated with
mutations in the SCNN1B gene.
These are: 1.
Multisystem pseudohypoaldosteronism, 2.
Liddle syndrome, and 3.
Cystic fibrosis-like disease. The disease...
- E3
ubiquitin ligase (CRL) complex.
Mutations in this gene
cause pseudohypoaldosteronism type IID (PHA2D); a rare
Mendelian syndrome featuring hypertension...
