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Ullrich-ähnliche kongenitale Muskeldystrophie ist eine autosomal rezessive Erkrankung
abnormal (hypermetric) gait
thromboembolic events and renal failure
high sensitivity to light
Dog is chocolate/liver brown (homozygous for brown colour) in eumelanin pigmented areas and carries at least two recessive alleles (identical or different)
Prekallikrein Defizienz option-set-443684-checkbox-1 Ullrich-ähnliche kongenitale Muskeldystrophie ist einePrekallikrein deficiency is an uncommon autosomal recessive disorder. It is a hemostatic disease characterized by deficiency of coagulation factor prekallikrein (PK). PK is a blood protein that is involved in the blood clotting process, so affected dogs experience prolonged activated partial thromboplastin time. The disease is usually asymptomatic with no signs of hematostatic defect in the absence of other blood clotting factor deficiencies, which
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