R609 Cholesterol Deficiency (CD)

R609 Categories: ,

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Sample material:  Blood EDTA, Blood Heparin, Hair, Semen, Tissue

10

working days

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Cholesterol deficiency (CD) is a genetic disorder found in Holstein cattle. The disorder impacts lipid metabolism that leads to chronic diarrhea and failure to thrive and eventually to the premature death of young calves. Calves affected by CD typically die within 3 weeks to 6 months of age, displaying significantly low cholesterol levels (severe hypocholesterolemia). These low cholesterol levels are caused by a mutation in the apolipoprotein B (APOB) gene, which plays a vital role in transporting fat molecules, including cholesterol, throughout the body and into cells.

Specifications

Chromosome: 11

Gene: APOB

Mode of Inheritance: Autosomal Recessive Lethal

Also known as: HCD, CDH

Organ: Multiple systems

Species:Cattle

Year published: 2016

Clinical Features

Affected calves show diarrhea and significantly low cholesterol levels (severe hypocholesterolemia). They usually die within 3 weeks to 6 months of age. Carriers of CD exhibit no obvious signs of malabsorption despite having reduced cholesterol levels compared to non-carriers.

References

Omia: 1965

Pubmed: 26763170