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===[[Congenital Panhypopituitarism]]===
 
===[[Congenital Panhypopituitarism]]===
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Also known as ''Pituitary Dwarfism'', Congenital Panhypopituitarism is defined by failure of differentiation of oesophageal ectoderm from which the pituitary is derived.  The pituitary is replaced by a cystic dilatation of ''Rathke's Cleft'' which replaces normal tissue with multilocular cysts- lined with non-secretory cuboidal epithelium. 
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[[Image:Pituitary dwarfism.jpg|right|thumb|125px|<small><center>'''Cystic Rathke's Pouch'''. Courtesy of A. Jefferies</center></small>]]
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''Incidence:''
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*Seen in German Shepherd Dog.  Inherited as a simple autosomal recessive trait in affected dogs. 
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*Congenital hypoplasia of the pituitary in the cat has also been reported.
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''Clinical signs:''
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Variable with degree of involvement of the pituitary.  Most obvious signs are due to the lack of [[Pituitary Growth Hormone - Anatomy & Physiology|GH]] during the growing phase of the puppy's life:
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*Pups appear normal at birth as the placenta supplies the foetus' need for GH.
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*Retarded growth and proportionate dwarfism.
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*Delayed growth plate closure; long bone physes normally close at 7-12 months but those of a pituitary dwarf will remain open until 3-4 years.
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*Delayed dental eruption.
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*Prognathism; undershot lower jaw as GH needed for mandible length.
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*Pups are quieter, more nervous and perhaps slower to learn. 
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*Retention of puppy coat; wooly.  Adult coat does not develop and a bilaterally symmetric, non-pruritic alopecia occurs over areas of friction E.g. neck and trunk. 
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*Hyperpigmentation with '''comedomes'''.
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*Reproductive signs E.g. failure to cycle, testicular atrophy.
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May also see signs of
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*Secondary hypothyroidism
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*Secondary hypoadrenocorticism
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''Diagnosis'':
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*Presumptive diagnosis based on signalment and clinical signs.
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*Radiography to detect growth plate closure.
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*'''GH stimulation test'''; Use alpha-2 agonist E.g. ''Xylazine'' which inhibit somatostatin and so induce GH production and release.  Normal dogs will have 2-4X increased GH after 20 mins while a pituitary dwarf will show little change in GH upon stimulation. 
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*'''Somatomedin Assay'''; Also called '''insulin-like growth factors'''.  GH mediates its effects by stimulating the production of IGFs which can be more easily measured.  Low levels will be found in pituitary dwarfs.
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*May also need to consider TSH and ACTH stimulation tests.
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''Treatment:''
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Need to treat early or will remain dwarfs. 
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*Sub-cut bovine/human GH can induce the growth of an adult haircoat.  <br>Nb. GH is '''diabetogenic''' so overdose will induce Diabetes Mellitus. 
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*Progestagens may induce GH production from the mammary gland.
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*May need to replace thyroid hormones and/or glucocorticoids.
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[[Category:Pituitary Gland - Pathology]]
       
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