Collie Eye Anomalie (CEA) Startseite Lysin und Arginin in Nieren

Lysin und Arginin in Nieren und Darm abnormal transportiert werden

macrothrombocytosis and variably shaped

The dog carries two copies of the recessive d allele and expresses diluted coat colour

Hypophosphatasia (HPP) is a rare canine autosomal recessive disease affecting bone and cartilage tissues

signs of keratoconjunctivitis sicca (KCS) from eyelid opening

Collie Eye Anomalie (CEA) Startseite Lysin und Arginin in NierenCollie eye anomaly (CEA, Choroidal Hypoplasia CH) is a hereditary eye disease in dogs, characterized by different level of impairment of the retina and choroid sclera that occurs during development of the eye. The inheritable disease is not progressive and the state after eye development remains stable. For this disease no drugs exist and it cannot be treated. The main symptom in affected dogs is hypoplasia (under development) of choroid, which is an