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Hundur Huntahvítfrumum viðloðun tegund Iii (CLAD3)


Canine Leukocyte Adhesion Deficiency Type III (CLAD3) is a rare genetic disorder affecting a dog’s immune system, leading to severe infections and poor wound healing. A DNA test for CLAD3 helps identify carriers and affected dogs, enabling responsible breeding decisions to prevent the spread of this condition. Early detection through genetic testing is crucial for managing the health of at-risk breeds. By using a reliable CLAD3 DNA test, breeders and veterinarians can improve canine health outcomes and reduce the incidence of this immune deficiency. Protect your dog’s future with accurate genetic screening for CLAD3 today. Stay informed and ensure your dog’s well-being with advanced DNA testing options.

Skammstöfun: CLAD3
Grein stökkbreyting: FERMT3 c.1349_1350insAAGACGGCTGCC
Erfðir: Autosomal víkjandi

Skammstöfun

CLAD3

Athuguð tíðni

Sjaldgæft

Klínísk alvarleiki

Alvarlegt

Klínísk flokkun

Ónæmisfræðilegir sjúkdómar

Greind stökkbreyting

FERMT3 c.1349_1350insAAGACGGCTGCC
p.(L450_A451insRRLP)

Erfðamáti

Autosomal víkjandi (Ljúkt)

Próf samantekt:

Canine Leukocyte Adhesion Deficiency Type III (CLAD3) is a rare genetic disorder affecting a dog’s immune system. It impairs the ability of white blood cells to adhere and migrate to infection sites, leading to severe and recurrent infections. A DNA test can identify carriers and affected dogs by detecting mutations responsible for CLAD3. Early diagnosis through testing helps breeders make informed decisions to reduce the spread of this condition. Managing affected dogs requires veterinary care to address infections and support immune function.

Fáanlegt úr pakkanum: Basic

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Understanding Canine Leukocyte Adhesion Deficiency Type III (CLAD3)

Canine Leukocyte Adhesion Deficiency Type III (CLAD3) is a genetic disorder that affects the immune system of dogs. This condition is characterized by a defect in the leukocyte adhesion process, which is critical for the proper functioning of the immune system. The deficiency disrupts the ability of white blood cells, or leukocytes, to adhere to blood vessel walls, preventing them from migrating to sites of infection or inflammation. As a result, affected dogs are more susceptible to infections and may experience chronic health issues.

Clinical Symptoms of CLAD3

Dogs with CLAD3 typically exhibit a range of clinical symptoms that are indicative of a compromised immune system. Common signs include recurrent infections, poor wound healing, and an increased frequency of inflammatory conditions. Affected dogs may also present with symptoms such as lethargy, fever, and swelling due to the inability of immune cells to effectively respond to pathogens.

Pathophysiology of CLAD3

The underlying cause of CLAD3 lies in a mutation within specific genes responsible for the production of adhesion molecules on leukocytes. These molecules are essential for the leukocyte's ability to stick to and traverse the endothelial cells lining blood vessels. When this adhesion process is impaired, the immune response is significantly weakened, leading to the clinical manifestations associated with the condition. This genetic mutation can lead to lifelong health challenges for affected dogs.

Diagnosis of CLAD3

Diagnosis of Canine Leukocyte Adhesion Deficiency Type III involves genetic testing to identify the specific mutation responsible for the condition. A DNA test can confirm the presence of the mutation, allowing for an accurate diagnosis. This diagnostic tool is particularly valuable for breeders and veterinarians, as it helps identify at-risk individuals and informs breeding decisions to reduce the prevalence of the disorder within certain populations.

Stjórnunar- og meðferðarúrræði

While there is currently no cure for CLAD3, management of affected dogs focuses on supporting their immune system and minimizing the risk of infections. This may include regular veterinary check-ups, prompt treatment of infections, and maintaining a clean environment to reduce exposure to pathogens. Additionally, owners may need to monitor their dogs closely for any signs of illness and seek veterinary care as needed.

Niðurstaða

Canine Leukocyte Adhesion Deficiency Type III is a serious genetic disorder that poses significant challenges for affected dogs due to their compromised immune function. Understanding the condition, recognizing its symptoms, and pursuing genetic testing are crucial steps in managing the health of dogs at risk. By raising awareness and educating dog owners and breeders, it is possible to mitigate the impact of this condition on canine health.


Tegund viðurkennd fyrir prófið: Huntahvítfrumum viðloðun tegund Iii (CLAD3)

  • American White Shepherd Dog
  • German Shepherd Dog
  • Shiloh Shepherd
  • Swiss White Shepherd Dog

🧬 Interpretation of genotypes CLAD3

Arfgerð
Staða
🟡 N/N
Ekki flutningsaðili - Engin áhætta
🟡 N/CLAD3
Flutningsaðili - Engin áhætta
❌ CLAD3/CLAD3
Fyrir áhrifum - í hættu

Algengar spurningar: skilja túlkunina

Hvað þýðir "Hreinsa"?

Dýrið ber ekki stökkbreytinguna. Það mun ekki þróa sjúkdóminn og mun ekki gefa það áfram.

Er „flutningsaðili“ alvara?

Nei. Dýrið er almennt heilbrigt en getur sent stökkbreytinguna til þess afkvæmi.

Hvað ef dýr hefur „áhrif“?

Það ber tvö stökkbreytt eintök. Búist er við klínískum einkennum eftir því sjúkdómnum. Það ætti ekki að rækta það.

Af hverju er munur á karli / konu?

Sumir sjúkdómar eru kyntengdir, þannig að tjáning þeirra er mismunandi eftir því kynlíf dýra.



Spáðu í afkvæmi

N/N (ekki-flutningsadili)
N/CLAD3 (Flytjandi)
CLAD3/CLAD3 (Fyrir áhrifum)

Algengar spurningar um DNA próf

Hvað greinir þetta DNA próf?

This DNA test detects the mutation associated with Canine Leukocyte Adhesion Deficiency Type Iii (CLAD3) in order to identify clear, carrier, or at-risk animals.

Af hverju að prófa ræktunardýr?

DNA próf hjálpar ræktendum að skipuleggja öruggari pörun og draga úr hættu á að stökkbreytingin berist til afkvæma.

Hver er arfleifð þessa prófs?

Erfðastillingin sem tilkynnt er um fyrir þetta próf er Autosomal Recessive.

Hvaða stökkbreyting er greind í þessu prófi?

This test analyses the mutation FERMT3 c.1349_1350insAAGACGGCTGCC.

Er burðardýr endilega fyrir áhrifum?

Ekki endilega. Túlkun fer eftir erfðamynstri og arfgerðinni sem myndast.


Heimildir

Boudreaux M K, Wardrop K J, Kiklevich V, Felsburg P, Snekvik K. A mutation in the canine Kindlin-3 gene associated with increased bleeding risk and susceptibility to infections. Thromb Haemost. 2010 Feb;103(2):475-7. doi: 10.1160/TH09-09-0571. Epub 2009 Nov 13.

Yfir 1400 erfðamerki yfir margar tegundir

Skoðaðu umfangsmikinn gagnagrunn með yfir 1.400 fullgiltum erfðamerkjum sem ná yfir hunda, ketti og hesta. Öflugur grunnur fyrir dýragreiningar og ábyrgar ræktunarákvarðanir.

Heill erfðamerkjagagnagrunnur

Fáðu aðgang að yfirgripsmiklum og faglega safnaðri gagnagrunni yfir erfðamerki, þar á meðal klínísk einkenni, greiningaraðferðir, meðferðarmöguleika, upplýsingar um stökkbreytingar, vísindalegar tilvísanir, viðurkenndar tegundir og stökkbreytingareiginleika.

Háþróuð erfðafræðileg verkfæri fyrir snjallari ræktunarákvarðanir

Taktu upplýstar ákvarðanir með öflugum erfðafræðilegum verkfærum sem eru hönnuð til að meta sjúkdómsáhættu, spá fyrir um feldlitarf, reikna skyldleikastuðla, sannreyna ætterni og líkana afkvæmum.

Hágæða greining með skjótum viðsnúningi

Njóttu góðs af háþróaðri rannsóknarstofugreiningu sem skilar áreiðanlegum og nákvæmum erfðafræðilegum niðurstöðum innan aðeins 1 til 2 vikna. Straumlínulagað vinnuflæði okkar og fullgiltar samskiptareglur tryggja skilvirkni án þess að skerða vísindalega strangleika.

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Huntahvítfrumum viðloðun tegund Iii (CLAD3)
Canine Leukocyte Adhesion Deficiency Type Iii (CLAD3) - MyLabDNA
Discover Canine Leukocyte Adhesion Deficiency Type III (CLAD3) DNA testing for dogs – accurate, reliable genetic health screening.
Huntahvítfrumum viðloðun tegund Iii (CLAD3)
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Canine Leukocyte Adhesion Deficiency Type Iii (CLAD3) - MyLabDNA
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Discover Canine Leukocyte Adhesion Deficiency Type III (CLAD3) DNA testing for dogs – accurate, reliable genetic health screening.
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