DOB 07.02.2022
PRAprcd A/; DNA test Progressive Retinal Atrophy (PRA-RCD4) N/N by parents
Osteochondrodysplasia (OC) N/N
Prcd mutation test for PRA N/N
Von Willebrand Disease (vWD) Type 1 N/N
DNA test Degenerative myelopathy(DM, SOD1A) N/N
Hips dysplasia C/C
Elbows 0/0
Patella lux 0/0
Eye examination- does not show symptoms of PRA, RD and cataract (HD) 17.07.23
PRAprcd A/; DNA test Progressive Retinal Atrophy (PRA-RCD4) N/N by parents
Osteochondrodysplasia (OC) N/N
Prcd mutation test for PRA N/N
Von Willebrand Disease (vWD) Type 1 N/N
DNA test Degenerative myelopathy(DM, SOD1A) N/N
Hips dysplasia C/C
Elbows 0/0
Patella lux 0/0
Eye examination- does not show symptoms of PRA, RD and cataract (HD) 17.07.23
Triin, 7 m.o.
8 month old
9 month old
15 month
17 month old
