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Addison's disease is
a rare but serious endocrine disorder in which the adrenal glands fail
to produce adequate amounts of essential hormones, particularly cortisol
and aldosterone. These hormones are crucial for maintaining blood
pressure, metabolism, immune function, and the body’s response to stress.
The condition often develops gradually and may go unnoticed until symptoms
become more severe.
Common causes include
autoimmune destruction of the adrenal cortex, infections, genetic
conditions, or damage due to medications or surgery. Symptoms typically
include chronic fatigue, muscle weakness, weight loss, low blood pressure,
salt cravings, and darkening of the skin (hyperpigmentation).
Patients may also experience nausea, abdominal pain, and dizziness, especially
when standing.
If left untreated,
Addison’s disease can lead to an adrenal crisis, a life-threatening
condition characterized by severe dehydration, low blood pressure, and shock. Prompt
medical attention is essential in such cases.
Diagnosis involves blood
tests to measure hormone levels and assess adrenal function, along with imaging
studies if needed. Treatment primarily includes lifelong hormone replacement
therapy to restore normal hormone levels. With proper management and regular
monitoring, individuals can lead healthy and active lives.