Milk-alkali Burnett syndrome is a rare genetic disorder that causes dysfunction of the thyroid gland. It is characterized by increased production of thyroid hormones (thyroxine and triiodothyronine) and can lead to serious health consequences.
Symptoms of Milk-Alkali Burnett Syndrome may include an overactive thyroid gland, which may manifest as tachycardia (fast heartbeat), increased blood pressure, metabolic problems, and other symptoms.
Treatment for milk-alkali Burnett syndrome involves the use of medications to lower thyroid hormone levels and prevent possible complications. However, despite treatment, many patients with this syndrome continue to experience symptoms that can impair quality of life.
Milk-alkali Burnett syndrome is a genetic disease that is inherited and can affect anyone, regardless of gender or age. Therefore, if you have family members with this condition, it is important to see a doctor for diagnosis and treatment.