Page 147 - Aussie Magazine no1, 2023
P. 147

A                B                C



          myelodysplastic syndromes. Diagnosis is made based
          on  characteristic  appearance  of  white  blood  cell
          nuclei identified by a blood smear. Most individuals
          with PHA do not require treatment as they do not       D                E                F
          have symptoms.


          The diagnosis of PHA is based on the morphologic
          characteristics  of  the  neutrophils  observed  on
          peripheral blood film examination. When a complete
          blood  count  (CBC)  is  requested,  digital  analysers
          will report a shift to the left without identifying the   GRADING PODLE BOWLESE
          specific anomaly of the neutrophils.
                                                                A – neutrofil, grade 1  D – neutrofil, grade 4
          The  heterozygous  version  is  more  common  and  is   B – neutrofil, grade 2  D – neutrofil, grade 4
          recognised  because  the  dog's  mature  neutrophils   C – neutrofil, grade 3  F – monocyt, hypolobulace
          resemble  bands  (slightly  immature  neutrophils)
          and  metamyelocytes  (a  predecessor  of  granular
          leukocytes). Heterozygous anomaly is not associated   PHA  status  of  breeding  dogs  can  be  determined
          with  immunodeficiency,  with  predisposition  to    by  examination  of  a  blood  smear  by  a  veterinary
          infection,  or  with  abnormalities  of  leukocyte  (white   pathologist.  Most  PHA  carriers  have  minor
          blood  cell)  function.  Conversely,  the  homozygous   anomalies in some of their blood cells.  However,
          anomaly is usually lethal in utero. Dogs that survive   not every PHA carrier will exhibit these anomalies
          may have leukocytes with round to oval nuclei on a   so  it  is  possible  to  receive  false  negative  results
          stained blood smear.                                 from  this  test.  Therefore,  any  breeding  dog  with
                                                               near  relatives  known  to  be  PHA  carriers  should
          The condition is inherited as an incomplete dominant.    be tested. PHA carrier dogs should not be bred to
          Dogs with only one gene are almost always healthy,   each other. If a breeding dog has extremely variable
          but  if  bred  to  another  carrying  the  mutation  the   litter sizes it may be a PHA carrier and should be
          pups that receive two copies of the PHA gene will    screened.
          be  reabsorbed,  stillborn  or  die  shortly  after  birth.
          Occasionally  a  puppy  will  survive  but  have  severe   In most cases, veterinarians discover the anomaly
          skeletal deformities and be susceptible to infection.  in  your  dog  by  accident  while  conducting  routine
                                                               blood tests. On a stained blood smear, nuclear hypo
          PHA is more of breeder’s problem than an owner's     segmentation of neutrophils, eosinophils, basophils,
          problem,  as  puppies  with  two  copies  of  the  PHA   and monocytes will be visible, whereby the nucleus
          gene almost never survive, and if they do, they will   of the cells has only two lobes or no lobes at all.
          have severe health issues. PHA causes small litters   The  hereditary  nature  of  disease  is  revealed  by
          or loss of new-borns.                                examination  of  blood  smears  from  parents  and
                                                               siblings. But of course, you can ask your vet to check
          The  PHA  gene  has  not  yet  been  found;  but  the   your Aussie for PHA.





















                                                                           A Worldwide Magazine for the Aussie  •  Issue 1/2023  |  147
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