Hypokalaemia

LABOKLIN Service ID: 8453

Burmese hypokalaemia, also known as familial episodic hypokalaemic polymyopathy, is a recessive genetic defect characterized by episodes of low serum potassium levels and high CPK (creatine phosphate kinase, an enzyme that indicates muscle damage). Clinical signs include episodes of skeletal muscle weakness which can affect the whole animal or may be restricted to certain muscles. This is most obvious in the neck muscles, but sometimes occurs in just the limbs. As a result affected cats may show problems with walking and holding their head correctly. The disease is not typically fatal and affected cats usually can be managed by adding potassium supplements to their diet. For specifics on management of this condition, owners are urged to consult with their veterinarian.

Method	TaqMan SNP assay
Breed list	Australian Mist, Burmese, Burmilla, Cornish Rex, Devon Rex, Singapura, Sphynx, Tonkinese
Heredity	autosomal recessive
Duration	3 - 5 days after arrival of the sample in the lab