What does CBS mean in BRITISH MEDICINE


Bartter syndrome is a rare inherited disorder characterized by a loss of salt and water, leading to dehydration and electrolyte imbalance. The condition has been classified into five types, one of which is known as CBCS or classic Bartter syndrome.

CBS

CBS meaning in British Medicine in Medical

CBS mostly used in an acronym British Medicine in Category Medical that means classic Bartter syndrome

Shorthand: CBS,
Full Form: classic Bartter syndrome

For more information of "classic Bartter syndrome", see the section below.

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Essential Questions and Answers on classic Bartter syndrome in "MEDICAL»BRITMEDICAL"

What is classic Bartter syndrome?

Classic Bartter syndrome (CBS) is an autosomal recessive disorder that causes dehydration, hypokalemic metabolic alkalosis and hypercalciuria due to an impairment of the kidneys' ability to reabsorb sodium and chloride from the tubules.

What are the symptoms of CBS?

Common signs and symptoms associated with CBS include failure to thrive in infancy, low blood potassium (hypokalemia), dehydration, urinating more than usual (polyuria), salt craving, nausea, vomiting and abdominal discomfort. People may also experience weakness in their muscles or feel lightheaded or dizzy due to low levels of potassium in their bloodstream.

Who is at risk for developing CBS?

As it is an inherited disorder with autosomal recessive inheritance pattern, CBS typically affects people whose parents both carry one mutated gene related to CBS on each chromosome they inherit from each parent.

How is CBS treated?

Treatment for CBS typically involves increasing fluid intake through IV fluids if needed; taking medications such as diuretics or thiazides; diet modification; supplements such as potassium and magnesium; and monitoring electrolyte levels regularly. In some cases, surgery may be necessary if there are structural abnormalities present in the kidneys that cause impaired filtration efficiency.

Final Words:
Classic Bartter syndrome (CBS) is a rare genetic disorder that affects the kidneys' ability to regulate salt and water balance in the body resulting in dehydration, electrolyte imbalance and hypokalemia among other symptoms if left untreated. It can only be inherited from two carriers of the gene mutation who both have one mutated gene on each chromosome they inherit from each parent. Treatment for this condition includes measures such as increasing fluids intake through IV fluids, taking medications, dietary modifications and supplementing with potassium & magnesium.

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