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K865 CombiBreed Genetic Diseases

Background

This combination package includes DNA-tests for:
K386 Mucopolysaccharidosis I
K504 Periodic paralysis (WNK4 - Hypokalemia)
K597 Congenital Adrenal Hyperplasia
K598 Dihydropyrimidinase Deficiency
K599 Hyperlipoproteinaemia
K600 Niemann-Pick C1 Disease
K601 Primary Hyperoxaluria II
K640 Gangliosidosis, GM2, type II - 1
K641 Vitamin D-deficiency rickets, type I
K646 Gangliosidosis, GM2, GM2A
K647 Gangliosidosis, GM2, type II - 2
K649 Hypothyroidism
K650 Mucopolysaccharidosis VII
K651 Mucopolysaccharidosis VI
K656 Haemophilia B - 1
K657 Haemophilia B - 2
K711 Polycystic Kidney Disease (PKD)
K725 Hypertrophic Cardio Myopathy 1 (HCM1)
K751 Glycogentoxicosis GSD Type IV
K754 Pyruvaatkinase Deficiency (PKDef)
K762 Progressive Retinal Atrophy (rdAc-PRA)
K767 Spinal Muscular Atrophie (SMA)
K793 Bloodtyping AB (DNA test)
K799 Hypertrophic Cardio Myopathy 3 (HCM3)

A small possibility exists that one or two tests which are part of a combination package will not provide results. Because of the low pricing of the combination packages, we cannot retest a single marker if this marker fails in a combination package.

If a particular test is highly important to you, we recommend that you order such a marker as a single test in our webshop. If needed, repeated testing is routinely performed on all single tests without extra costs.

Please refer to our FAQ-section for a further explanation.

Test specific information

Dr. van Haeringen Laboratorium B.V. (VHL), introduces a different strategy for DNA tests for several genetic markers. Recently, technical improvements have allowed for the combination of several genetic markers in one test.

Several tests are available in different breeds. For the different mutations, clinical studies linking a mutation to HCM are not always available. It is up to the owner to decide which test to perform.

Based on a recent inventory at other laboratories, we have learned that the test for HCM2 is not offered internationally. Consequently, we have contacted researchers in the USA. Based on our current information, we have decided to remove the HCM2 test as of the end of February 2012 from the Combination Package for Hereditary Diseases. For the moment, the HCM2 test remains available as a separate test.

Age

Information on individual tests is elsewhere available at www.vhlgenetics.com.

Throughput

Normally the result can be expected within 10 working days. This turn-around-time starts when both the sample and the fully filled-out and signed submission form have been received.

Location of disease or trait

Information on individual tests is elsewhere available at www.vhlgenetics.com.

Breed dependence

For this test samples from all breeds are accepted.

Sample type

For this DNA test we accept the following materials: Blood EDTA, Blood Heparin, Tissue, Swab. Please contact Dr. Van Haeringen Laboratorium if you wish to submit other material as listed.

Result

Information on individual tests is elsewhere available at www.vhlgenetics.com.

Inheritance

Information on individual tests is elsewhere available at www.vhlgenetics.com.

Severity of Disease

Information on individual tests is elsewhere available at www.vhlgenetics.com.

 
Cat

CombiBreed Genetic Diseases

Code K865
€ 66,55 (incl. 21% VAT)
€ 55,00 (excl. VAT)
Quantity