Primäre Ziliäre Dyskinesie (PCD) - Bobtail option-set-443684-checkbox-1 Allele at is responsible for

Allele at is responsible for black-and-tan or tricolor phenotype

Mutation: CDH23 gene

Mutations altering the sequence can lead to disruptions of the collagen structure

characterized by a pattern of distinctive black patches on a white background

secondary hyperparathyroidism

Primäre Ziliäre Dyskinesie (PCD) - Bobtail option-set-443684-checkbox-1 Allele at is responsible forPrimary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder characterized by abnormally functioning cilia. The main clinical signs are recurrent or persistent respiratory infections because of the lack of effective ciliary motility. Other clinical signs include left right body asymmetry due to disruption of embryonic development and impaired male fertility due to defects of the spermatozoa flagella. Primary ciliary dyskinesia (PCD) is an