ABSTRACT A young female French bulldog with a history of chronic right keratoconjunctivitis sicca (KCS) because since birth was referred for an acute onset of nonambulatory tetraparesis. Right trigeminal nerve sensory deficits, including right corneal anesthesia and absent facial sensation, were identified during examination. Magnetic resonance imaging (MRI) of the neurocranium was performed, revealing severe hypoplasia to the absence of the right trigeminal ganglion, consistent with reports of congenital trigeminal hypoplasia/aplasia in human medicine. This represents a very rare but important differential in young patients with a history of non‐responsive KCS, recurrent or slow healing corneal ulceration, and absent corneal sensation.
Jarvis et al. (Sat,) studied this question.