- Akita
- ACPT
- Système digestif
Amelogenesis Imperfecta (AI) – Akita
€57,48 €47,50 excl. BTW
Description
Amelogenesis Imperfecta (AI), also known as Familial Enamel Hypoplasia (FEH), represents a heterogeneous group of inherited disorders affecting tooth enamel. The condition uniformly affects deciduous and permanent teeth and is manifested by enamel roughening/thinning and brownish mottling.
This variant of the disorder, also known as Amelogenesis Imperfecta 3, is found in the Akita Inu. It is caused by a recessive mutation to the gene ACPT (also known as ACP4).
Informations complémentaires
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue, Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
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