€57,48 €47,50 IVA esclusa
Amelogenesis Imperfecta (AI), also known as Familial Enamel Hypoplasia (FEH), represents a heterogeneous group of inherited disorders affecting tooth enamel.
Working days 10
Specifiche
Breeds | |
---|---|
Gene | |
Organ | |
specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
Mode of Inheritance | |
Chromosome | |
Also known as | |
Year Published |
Informazioni generali
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 is caused by a recessive mutation to the gene ENAM, and is found in the Parson Russell Terrier and Jack Russell Terrier.
Caratteristiche cliniche
I denti interessati sono spesso piccoli e appuntiti con maggiori lacune. Nessun organo o tessuto diverso dai denti è affetto da questa malattia. L'Amelogenesis Imperfetta (AI) può essere classificata in tipi ipoplastici, ipomaturanti e demineralizzati.
Informazioni aggiuntive
Riferimenti
Pubmed ID: 30877375
Omia ID: 1805