Introduction
- Extremely rare.
- Cause : congenital hereditary disorder of leukocyte development.
- Signs : may be evidence of low-grade infection.
- Diagnosis : often incidental finding of apparent continual left shift despite animal appearing clinically normal.
- Treatment : none, supportive care only if evidence of infection.
- Prognosis : survival times not reported but animals probably can live relatively normal lives.
Diagnosis
Clinical signs
- No clinical signs specific to disease.
Diagnosis
Differential diagnosis
Sequelae
Prognosis
- Prognosis may be quite good as many individuals reach adulthood without diagnosis.
Sources
Publications
Refereed papers
- Latimer K S, Rowland G N & Mahaffey M B (1988)Homozygous Pelger-Huet anomaly and chondrodysplasia in a stillborn kitten.Vet Pathol25, 325-328.
- Guildford W G (1987)Primary immunodeficiency diseases of dogs and cats.Comp Cont Educ Prac Vet9, 641-50. (Useful review of feline immunodeficiency.)
- Latimer K S, Rakich P M & Thompson D F (1985)Pelger-Huet anomaly in cats.Vet Pathol22, 370-374.
- Weber S E, Evans D A & Feldman B F (1981).Pelger-Huet anomaly of granulocytic leukocytes in two feline littermates.Feline Practice11, 44-47. (Original report of the anomaly in cats.)




