fbpx

Gallbladder Mucocele H360

56,87 € each

*
*

Background

This disease is characterized by formation of gallbladder mucoceles (cysts).

Test specific information

-

Age

?Late onset? ? This phrase indicates, that the symptoms of the disease can be detected at a later ages. ?Late onset? is the opposite of ?early onset?, in which symptoms may be present at younger ages. The phrases are used because the mutation causing ?late onset? symptoms may be different compared to the mutations causing ?early onset? symptoms.

Throughput

Normally the result can be expected within 15 working days. This turn-around-time starts when both the sample and the fully filled-out and signed submission form have been received.

Location of disease or trait

This disease is present in the entire body, but causes main effects in the internal organs such as stomach, intestinal tract, liver and / or kidneys. In a number of cases, the disease affects one major internal organ.

Breed dependence

This DNA test is available for the following breeds: Cairn Terrier, Cocker Spaniel, Pomeranian, Sheltie.

Sample type

For this DNA test we accept the following materials: Swab, Tissue, Semen, Blood EDTA, Blood Heparin. Please contact PharmaDNA if you wish to submit other material as listed.

Result

An animal can be free and has in that situation two healthy alleles. When used in breeding this animal will not become ill due to the disease. It cannot spread the disease in the population. An animal can be carrier and has in that situation one healthy and one disease allele. When used in breeding 50 percent of the offspring will receive the disease allele. Carriers will also become ill. An animal can be affected and has in that situation two disease alleles. When used in breeding all offspring will also receive the disease allele. Affected will also become ill.

Inheritance

This genetic factor is inherited in an autosomal, dominant, mode. This means, that the individual can be free of the mutation (homozygote normal), affected (homozygous affected) or carrier (heterozygous affected). Both carriers and affected individuals will show symptoms of the mutation.

Severity of Disease

-