Search: H673 Degenerative Myelopathy, DM – Page 3

Neuronal Ceroid Lipofuscinosis 5 (NCL5)

Neuronal Ceroid Lipofuscinosis (NCL) is the name for a wide array of degenerative neurological conditions which cause progressive nerve damage, resulting in a loss of mobility and vision, and ultimately...

Cerebellar Abiotrophy (CA) – Kelpie

Cerebellar Abiotrophy is a hereditary neurodegenerative disorder affecting the cerebellum. The cerebellum is the part of the brain responsible for balance, coordination, and fine motor control. In Kelpies this condition...

Neuronal Ceroid Lipofuscinosis 6 (NCL6) – Schapendoes

Neuronal Ceroid Lipofuscinosis 6 (NCL6) is a hereditary neurodegenerative lysosomal storage disorder caused by mutations in the ceroid‑lipofuscinosis neuronal 6 (CLN6) gene. This defect leads to the build‑up of lipopigments,...

Gangliosidosis (GM2 Type II) – Cat All Breeds

Gangliosidosis (GM2 Type II) is a fatal, progressive neurodegenerative disease caused by mutations in the HEXA and HEXB genes. These mutations lead to a deficiency of an enzyme that is...

Cortical Cerebellar Abiothrophy (NCCD) – Vizsla

Cerebellar cortical degeneration (CCD) is a neurodegenerative disease process affecting many dog breeds. The disease affects a specific area of the brain known as the cerebellum. In cerebellar degeneration, the...

Gangliosidosis (GM2 Type I) – Japanese Chin

Gangliosidosis (GM2 Type I) is a fatal, progressive neurodegenerative disease caused by mutations in the HEXA and HEXB genes. These mutations lead to a deficiency of an enzyme that is...

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