VNDD
  • Home
  • Search
  • Contact
  • More
    • Methodology
    • Video Library
    • External Resources
    • FAQ
<Return to Disease List
Holoprosencephaly
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
<
>
Holoprosencephaly is a malformation of the forebrain characterized by the absence of two separate cerebral hemispheres and midline structures, due to incomplete separation, and the development of hydrocephalus
Age of Onset: Less than 2 months of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over time
Clinical Signs:
Behavioral/Mental Awareness
Intermittent resource guarding (food) 
Inappropriate vocalization
Altered mentation (ranged from lethargic to spastic and aggressive)

Lethargy
Coprophagia
Hypodypsia (with hypernatremia)
​Pica


Movement
Ataxia
Circling 
Slight forelimb hypermetria

Special Functions (e.g. respiration; urination)
Intermittent coughing

Other
Other congenital developmental abnormalities (cryptorchidism, retained deciduous teeth, hypoplastic penis)
Intracranial- supratentorial
Unknown
To read more about this disease click below:
References
Picture
Contact us:
[email protected]

Privacy Policy
Terms and Conditions​
Disclaimer
  • Home
  • Search
  • Contact
  • More
    • Methodology
    • Video Library
    • External Resources
    • FAQ