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X-linked hypohidrotic ectodermal dysplasia is a disease characterised by missing or malformed teeth and absent sweat glands. The disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

Congenital myasthenic syndrome, also known as spasticity, is a disease causing congenital muscle weakness. Affected cats frequently adopt a characteristic squirrel-like position by resting their front paws on an object. Signs of the disease appear at about 3 weeks of age. The disease can progress slowly but affected individuals usually die before 2 years of age.

This package includes the mandatory tests defined by the Flemish breeding program for Miniature Spitz: Type 2 degenerative myelopathy (DOG-DM2),  progressive degeneration of rods and cones (DOG-PRA-PRCD), progressive retinal atrophy (NECAP1) (DOG-PRA-NECAP1) and Von Willebrand disease type 1 (DOG-VWD1).

The Flemish breeding program also recommends the tests included in DOG-POM-VL+ pack.

This package includes the mandatory tests defined by the Flemish breeding program for Parson Russell Terrier: (DOG-AI), Degenerative myelopathy 2 (DOG-DM2), Juvenile encephalopathy / early-onset epilepsy (DOG-JBD), Late-onset spinocerebellar ataxia (DOG-LOA), Primary lens luxation (DOG-PLL) and Spinocerebellar ataxia (DOG-SCA). The Flemish breeding program also recommends the test Collie eye anomaly (DOG-CEA).

This package includes the mandatory tests defined by the Flemish breeding program for Chinese Crested Dog : primary lens luxation (DOG-PLL), progressive rod-cone degeneration (DOG-PRA-PRCD), rod-cone dysplasia 3 (DOG-PRA-RCD3) and degenerative myelopathy 2 (DOG-DM2).

The Flemish breeding program also recommends the tests included in our DOG-CHINESE-VL+ pack.

This pack includes the mandatory tests defined by the Flemish breeding program for Miniature German Spitz: Type 2 degenerative myelopathy (DOG-DM2), progressive retinal atrophy (DOG-PRA-PRCD), progressive retinal atrophy (NECAP1) (DOG-PRA-NECAP1), and Von Willebrand disease type 1 (DOG-VWD1).

The Flemish breeding program also recommends the tests included in our DOG-SPIA-P-VL+ pack.

This package includes the mandatory tests defined by the Flemish breeding program for Golden Retriever: progressive retinal atrophy type 1 (DOG-PRA1-GR), progressive retinal atrophy type 2 (DOG-PRA2-GR), ichthyosis (DOG-ICHGR) and progressive degeneration of rods and cones (DOG-PRA-PRCD).

The Flemish breeding program also recommends the tests included in our DOG-RETRIERVER-VL+ pack.

Haemophilia B, also known as factor IX deficiency, is a bleeding disorder. The clinical signs are haematomas and excessive bleeding due to the absence of functional coagulation factor IX.  he disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

Myotubular myopathy type 1, also known as X-linked myotubular myopathy, is a genetic disease of the skeletal muscles. Clinical signs include hypotonia, muscle atrophy and breathing difficulties. The disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

This package includes the mandatory tests defined by the Flemish breeding program for American Staffordshire Terrier: degenerative myelopathy type 2 (DOG-DM2), neuronal ceroid lipofuscinosis 4A (DOG-NCLA), progressive retinal atrophy type 4 (DOG-PRA-CRD4) and progressive retinal atrophy type 1 (DOG-PRA-RCD1).

The Flemish breeding program also recommends the tests included in our DOG-AMSTAFF-VL+ pack.