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Pseudohypoaldosteronism type 1, autosomal dominant

Pseudohypoaldosteronism type 1, autosomal dominant: Introduction

Pseudohypoaldosteronism type 1, autosomal dominant: A rare condition characterized by electrolyte disorders caused by the kidney's inability to respond to mineralocorticoids. Type 1 is differentiated from type II in that it involves sodium wasting. There are two forms of type 1: an autosomal recessive form which tends to be more severe than the autosomal dominant form. The recessive form tends to persist into adulthood whereas the dominant form is milder and symptoms tend to improve with age. More detailed information about the symptoms, causes, and treatments of Pseudohypoaldosteronism type 1, autosomal dominant is available below.

Symptoms of Pseudohypoaldosteronism type 1, autosomal dominant

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Pseudohypoaldosteronism type 1, autosomal dominant: Complications

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Causes of Pseudohypoaldosteronism type 1, autosomal dominant

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Pseudohypoaldosteronism type 1, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Pseudohypoaldosteronism type 1, autosomal dominant

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Prognosis for Pseudohypoaldosteronism type 1, autosomal dominant

Prognosis for Pseudohypoaldosteronism type 1, autosomal dominant: responds well to salt intake

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Definitions of Pseudohypoaldosteronism type 1, autosomal dominant:

A heterogeneous group of disorders with common symptoms of apparent HYPOALDOSTERONISM despite the elevated levels of ALDOSTERONE and RENIN. Other clinical symptoms include HYPERKALEMIA with (Type I) or without (Type II) sodium wasting. Pseudohypoaldosteronism can be the result of defective MINERALOCORTICOID RECEPTORS or defects in the epithelial SODIUM CHANNEL. It can also be acquired after KIDNEY TRANSPLANTATION. - (Source - Diseases Database)

Pseudohypoaldosteronism type 1, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Pseudohypoaldosteronism type 1, autosomal dominant, or a subtype of Pseudohypoaldosteronism type 1, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Pseudohypoaldosteronism type 1, autosomal dominant

  1. Pseudohypoaldosteronism type 1, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis
 

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