Where Dog Breed fantasy Goes to Die.
Persistent hyperplastic primary vitreous is a congenital ocular developmental anomaly in which fetal vitreous and vascular tissue fail to regress normally, causing lens, vitreous, and retinal abnormalities that may impair vision.
Comments closedPneumonia is inflammation and infection or aspiration-related injury of the lung parenchyma and lower airways, causing impaired gas exchange, respiratory distress, cough, fever, and systemic illness.
Comments closedGUCY2D-PRA is a breed-associated genetic form of progressive retinal atrophy involving the GUCY2D gene, which is important for normal photoreceptor signaling and retinal function.
Comments closedIFT122-PRA is a genetic form of progressive retinal atrophy associated with the IFT122 gene, which is involved in ciliary transport and normal photoreceptor maintenance.
Comments closedPRA-rcd2 is a specific inherited form of progressive retinal atrophy causing degeneration of retinal photoreceptors, usually leading to progressive vision loss and eventual blindness.
Comments closedPRA-rcd4 is a specific inherited form of progressive retinal atrophy causing degeneration of retinal photoreceptors, usually leading to progressive vision loss and eventual blindness.
Comments closedVon Willebrand disease Type III is a severe inherited von Willebrand factor deficiency in which von Willebrand factor is absent or nearly absent, causing marked impairment of primary hemostasis and high risk of serious bleeding.
Comments closedCanine multifocal retinopathy 2 is an inherited retinal disorder classified as a specific CMR subtype, with breed-specific genetic testing and retinal lesion documentation requiring current laboratory verification.
Comments closedCanine multifocal retinopathy 3 is an inherited retinal disorder classified as a specific CMR subtype, with breed-specific genetic testing and retinal lesion documentation requiring current laboratory verification.
Comments closedPanosteitis is a self-limiting inflammatory disease of the long bones in young dogs, characterized by episodic shifting lameness, pain on long-bone palpation, and radiographic medullary changes.
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