LITTLE SHADOW RETRIEVERS
DAMES
Piper 1/25/21
OFA(Hips)- Good
OFA(Elbows)- normal
embark genetic testing:
Cainine Elliptocytosis- clear
Pyruvate Kinase Deficiency- clear
PRCD exon 1- carrier
GR-PRA2 - clear
progressive retinal atrophy, CRD4/cord1 - clear
day blindness- clear
Macular Corneal Dystrophy- clear
Urate Kidney and bladder stones- clear
Alexander disease- clear
Narcolepsy- clear
Ullrich-like congenial muscular dystrophy- clear
Centronuclear myopathy, CNM- clear
Exercise-induced collapse EIC- clear
X-linked myotubular myopathy-clear
Congenial myasthenic syndrome, CMS- clear
hereditary nasal parakeratosis, HNPK- clear
Skeletal dysplasia 2, SD2- Clear
Dalia(future breeder)
OFA(Hips)- tbd (she is still to young)
OFA(Elbows)-
Embark genetic testing:
Cainine Elliptocytosis- clear
Pyruvate Kinase Deficiency- clear
PRCD exon 1- clear
GR-PRA2 - clear
progressive retinal atrophy, CRD4/cord1 - clear
day blindness- clear
Macular Corneal Dystrophy- clear
Urate Kidney and bladder stones- clear
Alexander disease- clear
Narcolepsy- clear
Ullrich-like congenial muscular dystrophy-clear
Centronuclear myopathy, CNM- clear
Exercise-induced collapse EIC- clear
X-linked myotubular myopathy-clear
Congenial myasthenic syndrome, CMS-clear
hereditary nasal parakeratosis, HNPK-clear
Skeletal dysplasia 2, SD2-clear
Lavi
OFA(Hips)- tbd (she is still to young)
OFA(Elbows)-
Embark genetic testing:
Cainine Elliptocytosis- clear
Pyruvate Kinase Deficiency- clear
PRCD exon 1- clear
GR-PRA2 - clear
progressive retinal atrophy, CRD4/cord1 - clear
day blindness- clear
Macular Corneal Dystrophy- clear
Urate Kidney and bladder stones- clear
Alexander disease- clear
Narcolepsy- clear
Ullrich-like congenial muscular dystrophy-clear
Centronuclear myopathy, CNM- clear
Exercise-induced collapse EIC- clear
X-linked myotubular myopathy-clear
Congenial myasthenic syndrome, CMS-clear
hereditary nasal parakeratosis, HNPK-clear
Skeletal dysplasia 2, SD2-clear
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Kyrie(future breeder)
OFA(Hips)- tbd (she is still to young)
OFA(Elbows)-
Embark genetic testing:
Cainine Elliptocytosis- clear
Pyruvate Kinase Deficiency- clear
PRCD exon 1- clear
GR-PRA2 - clear
progressive retinal atrophy, CRD4/cord1 - clear
day blindness- clear
Macular Corneal Dystrophy- clear
Urate Kidney and bladder stones- clear
Alexander disease- clear
Narcolepsy- clear
Ullrich-like congenial muscular dystrophy-clear
Centronuclear myopathy, CNM- clear
Exercise-induced collapse EIC- clear
X-linked myotubular myopathy-clear
Congenial myasthenic syndrome, CMS-clear
hereditary nasal parakeratosis, HNPK-clear
Skeletal dysplasia 2, SD2-clear