LABOKLIN (UK)|Genetic Diseases | Dogs| von-Willebrand disease type II (vWD II)
prices in Pound
  Home
  Avian DNA Tests
  Genetic Diseases
Dogs
Cats
Horses
Cattle
Pigs
  Coat Colours / Length
  Identity / Parentage
  Order Online
  About Us
  Contact Us
 
von-Willebrand disease type II (vWD II)
Breed
German Wirehaired Pointer .
The Disease
von-Willebrand disease is an inherited bleeding disorder, which is highly heterogeneous ranging from an asymptomatic laboratory abnormality to a life threatening bleeding. The condition is caused by a quantitative or qualitative deficiency of von Willebrand factor (vWF). Von Willebrand's disease vWD Type II affects The German wirehaired pointer and cause severe bleeding disorder.
Trait of Inheritance
Type II vWD is very uncommon. It is an autosomal recessive trait.

Inheritance : AUTOSOMAL RECESSIVE trait


 

Sire

  Dam   Offspring
         
Clear
x
Clear
>
100% Clear
         
clear
x
carrier
>
50%  Clear + 50% carriers
         
clear
x
affected
>
100% carriers
         
carrier
x
Clear
>
50%  Clear + 50% carriers
         
carrier
x
carrier
>
25% clear + 25% affected + 50% carriers
         
carrier
x
affected
>
50% carriers + 50% affected
         
affected
x
Clear
>
100%  carriers
         
affected
x
carrier
>
50% carriers + 50% affected
         
affected
x
affected
>
100% affected

 


Clear

Genotype: N / N [ Homozygous normal ]

The dog is noncarrier of the mutant gene.

The dog will never develop von-Willebrand disease type II (vWD II) and therefore it can be bred to any other dog.

 

Carrier

Genotype: N / vWD [ Heterozygous ]

The dog carries one copy of the mutant gene and one copy of the normal gene.

The dog will never develop von-Willebrand disease type II (vWD II) but since it carries the mutant gene, it can pass it on to its offspring with the probability of 50%.

Carriers should only be bred to clear dogs.

Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)

 

Affected

Genotype: vWD / vWD [ Homozygous mutant ]

 

The dog carries two copies of the mutant gene and therefore it will pass the mutant gene to its entire offspring.

The dog will develop von-Willebrand disease type II (vWD II) and will pass the mutant gene to its entire offspring
Sample Requirements
Whole blood in EDTA tube (0.5 - 1 ml) or Buccal Swabs.
Turnaround
withing 7 working days
Price
£ 65.96 (including VAT)

To order:

  • Download Order Form from this link pdf

  • Complete the order form and send it together with your samples to the following address:

    Laboklin (UK),   61 Mouldsworth Ave, Manchester M20 1GG

See Also:
Copper Toxicosis  
Degenerative Myelopathy  
Globoid Cell Leukodystrophy (Krabbe Disease)  
CSNB (Congenital Stationary Night Blindness)  
CLAD (Canine Leukocyte Adhesion Deficiency)  
Cystinuria  
PK Deficiency (Pyruvate Kinase Deficiency)  
Fucosidosis  
PFK Deficiency (Phosphofructokinase deficiency)  
Myotonia Congenita  
MH (Malignant Hyperthermia)  
X-SCID (X-Linked Severe Combined Immunodeficiency)  
GM1-Gangliosidosis  
Narcolepsy  
GRMD (Golden Retriever Muscular Dystrophy)  
MPS ( Mucopolysaccharidosis type VII)  
Hereditary Myopathy / Centronuclear Myopathy (HMLR, CNM)  
Canine Cyclic Neutropenia (Gray Collie Syndrome)  
cord1- PRA ( Cone-rod dystrophy 1 )  
prcd - PRA ( Progressive Retinal Atrophy )  
L-2-HGA ( L- 2 - hydroxyglutaric aciduria )  
von Willebrand disease Type I (vWD I)  
von Willebrand disease Type III (vWD III)  
Neuronal Ceroid Lepofuscinosis ( NCL )  
Trapped Neutrophil Syndrome ( TNS ) *  
crd PRA (Cone-rod dystrophy form of PRA)  
PDP 1 Deficiency (Pyruvate Dehydrogenase Phosphatase 1 Deficiency)  
Factor VII Deficiency  
rcd1 PRA (Progressive Retinal Atrophy)  
rcd3 PRA (Progressive Retinal Atrophy)  
rcd1a PRA (Progressive Retinal Atrophy)  
MDR1 Gene Defect / Ivermectin Sensitivity  
Exercise Induced Collapse ( EIC )  
Dwarfism (Pituitary Dwarfism / Hypopituitarism)  
PRA (Progressive Retinal Atrophy)  

 
 
Home   |   Avian DNA Tests  |   Genetic Diseases  |   Coat Colours / Length  |   Identity / Parentage  |   About us  |   Contact Us
LABOKLIN GmbH & Co. KG
ISO / DIN 17025 Accredited Laboratory
© 2007 Laboklin (UK)
61 Mouldsworth Ave, Manchester M20 1GG
Tel. 0161 282 3066