X-chromosomal Myotubuläre Myopathie (XL-MTM) - Rottweiler Rassebestimmung Mutation: C3 gene

Mutation: C3 gene

therefore its excess in urine forms crystals that lead to formation of cystine stones in kidney or bladder

GUTSCHEIN SCHENKEN

It allows full expression of colours defined by A-Locus

such as vaccination or viral infection

X-chromosomal Myotubuläre Myopathie (XL-MTM) - Rottweiler Rassebestimmung Mutation: C3 geneMyotubular myopathy is a X linked recessive disorder. Affected infant male puppies show signs of facial, axial and proximal neuromuscular weakness with tetraparesis, difficulty holding the head up and a dropped jaw, including hypotonia and areflexia leading to respiratory insufficiency and death within 2 weeks. The symptoms usually occur postnatal and progress very quickly. The affected male puppies have to be euthanised due to progressive symptoms.