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Kongenitale Dyshormonogene Hypothyreose mit Kropf (CDHG) Züchter Mutation: CDH23 gene

SKU: 79688796565
4.9

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Description

Mutation: CDH23 gene

ECLE commonly affects breeds of German Shorthaired Pointer

muscular fibrosis with fat infiltrations and cardiomyopathy

Banded hairs are usually present along the dorsal area of the torso

Kongenitale Dyshormonogene Hypothyreose mit Kropf (CDHG) Züchter Mutation: CDH23 geneCongenital dyshormonogenic hypothyroidism with goiter (CDHG) is an autosomal recessive disorder, caused by lymphocytic destruction or idiopathic atrophy of the thyroid gland. The clinical signs include growth delay, low intensity heart murmur, cough, exercise intolerance, goiter and dyshormonogenesis. Inheritance: autosomal recessive Mutation: SLC5A5 gene Genetic test: The method used for genetic testing is extremely accurate and allows complete

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