MSD Manual

Please confirm that you are a health care professional

honeypot link

Congenital and Inherited Cerebral Disorders in Animals

By

Rebecca A. Packer

, MS, DVM, DACVIM (Neurology), College of Veterinary Medicine and Biomedical Sciences, Colorado State University

Last full review/revision Sep 2020 | Content last modified Sep 2020
Topic Resources

Large Animals

Anencephaly means that the brain is largely absent at birth. It is a rare disorder but is seen sporadically in calves; the cause is unknown. Because the pituitary gland may also be absent, prolonged gestation Prolonged Gestation in Cattle and Sheep read more of affected calves can occur. Signs include profound lethargy, head pressing, and blindness with normal pupillary reflexes. Cerebral aplasia in calves is usually associated with complete absence of both cerebral hemispheres, and CSF may leak out of a small opening on the midline between the frontal bones.

Exencephaly means that the brain is exposed through a large defect in the skull (cranium bifida). The brain (encephalocele), meninges (meningocele), or both (meningoencephalocele) may protrude through this opening. Encephalocele and meningocele are seen in many species and are known to be inherited in pigs. There is some evidence that high doses of Vitamin A during pregnancy may cause exencephaly in some species.

Defects may be closed or open in terms of communication with the environment through skin defects. Too little information exists to reliably predict outcome and resolution of any deficits. Good surgical outcomes have been achieved in some case reports of closed meningoencephaloceles as the protruding tissue is generally not functional; however, improvement of existing clinical signs is not expected. The goal of surgical correction is to prevent further trauma or close any external communication. When considering treatment, safety must be considered, as with any ataxic, seizuring, or mentally inappropriate large animal. When the defects openly communicate externally, CNS infection should be presumed unless proven otherwise.

In hydranencephaly, there is a marked loss of cerebral cortical tissue (primarily the neocortex) within a cranial vault of normal conformation. The resultant cavity communicates with the ventricular system, has an incomplete ependymal cell lining, and is filled with CSF. Clinical signs may include lethargy, propulsive circling, head pressing, and blindness. Hydranencephaly develops as a result of the destruction of developing neural tissues and is sometimes accompanied by cerebellar hypoplasia and arthrogryposis. Hydranencephaly is seen sporadically or as an epidemic in calves, lambs, and less commonly in piglets.

Known causes include infection in utero with a number of viruses, including Akabane virus Akabane and Related Simbu Serogroup Virus Infections in Ruminants Akabane and related Simbu serogroup viruses are transmitted to ruminants by Culicoides midges. They cause congenital abnormalities of the CNS and musculoskeletal system in ruminants. Diagnosis... read more in ruminants in Australia, Japan, and Israel; bluetongue Bluetongue read more virus in sheep and cattle in North America; Rift Valley fever Rift Valley Fever read more virus and the virus of Wesselsbron disease Overview of Wesselsbron Disease Wesselsbron disease is an acute, arthropod-borne flavivirus infection of mainly sheep, cattle, and goats in sub-Saharan Africa. Infection is common, but clinical disease is infrequent although... read more in sheep and cattle in Africa; the Cache Valley virus Cache Valley Virus Also see Management of Reproduction: Sheep. Abortion in ewes, as in cows, is not always easily diagnosed. Although many of the toxins that cause abortion in cows also cause problems in ewes... read more in sheep in the USA; and the Chuzan virus in calves in Japan. Rarely, bovine viral diarrhea Bovine Viral Diarrhea and Mucosal Disease Complex Bovine viral diarrhea/mucosal disease is a pestivirus infection of cattle and other ruminants. Infection leads to immunosuppression and can cause signs in multiple body systems in addition to... read more and border disease virus Border Disease Border disease is observed in young ruminants exposed to border disease virus during gestation. Surviving lambs demonstrate failure to thrive, a long hair coat, and tremors, giving rise to the... read more produce hydranencephaly in lambs and calves. Hydranencephaly and porencephaly (cystic cavities in the cerebrum) are seen sometimes in lambs with in utero copper deficiency (swayback). It also is seen in a syndrome of prolonged gestation in sheep in Scotland (cause unknown).

Hydrocephalus, an increase in volume of the CSF, can appear similar to hydranencephaly, but in hydrocephalus the ventricles retain a complete ependymal lining. When born alive, affected animals often have a characteristic dome-shaped head, and may also have inappetence, seizures, lethargy and altered mental status. There may be extensive expansion of the lateral ventricles in the frontal lobes. Hydrocephalus is seen sporadically in all large animals, although it is relatively common in calves, in which inheritance and vitamin A deficiency have been implicated.

Cyclopia is characterized by a single orbital fossa. One cause in lambs is ingestion by the gestating dam of plant alkaloids from Veratrum californicum. This malformation also is seen in pigs.

Lissencephaly, an absence or reduction of cerebral gyri, is a rare disorder seen in Churra lambs. Lesions also include cerebellar hypoplasia. Clinical signs consist of weakness, inability to walk, difficulty suckling, and muscular rigidity. Clinical signs are apparent at birth. It is caused by a mutation in the RELN gene.

Idiopathic or familial epilepsy has been described in many species. Benign epilepsy is seen in young foals, particularly Arabians, up to 12 months of age. The foal may present for seizures, head injuries, or postictal blindness. Foals usually recover spontaneously within a few months, but anticonvulsant therapy (phenobarbital, 100–500 mg, PO, twice daily, for a 50-kg foal) is probably advisable for 1–3 months, followed by withdrawal over 2 weeks. Epilepsy beginning by 1 year of age has been recorded in Brown Swiss and Swedish Red cattle. Seizures are also seen in young Aberdeen Angus calves; if these calves survive, they show cerebellar signs but become clinically normal by 2 years of age.

Metabolic disorders and lysosomal storage disorders often cause signs of forebrain dysfunction, along with other neurologic deficits, and are discussed further under multifocal disorders Congenital and InheritedMultifocal Disorders of the Nervous System in Animals Shaker calf syndrome is a neurodegenerative disorder that is seen in Hereford calves. Affected animals show a marked tremor within hours of birth, difficulty in rising, a stiff gait, and loss... read more . Cerebral signs seem to be most prominent in citrullinemia.

Citrullinemia is a fatal, autosomal recessive, metabolic defect of Holstein-Friesian calves (mainly in Australia and New Zealand) associated with cerebral cortical edema. It is due to increased citrulline in plasma, caused by deficiency of the urea cycle enzyme argininosuccinate synthetase. Affected calves appear healthy at birth but die of acute neurologic disease in 1–4 days. Signs are sudden in onset and consist of depression, aimless wandering, blindness, seizures, opisthotonos, and recumbency.

Narcolepsy, a disorder of sleep-wake control (typically characterized by excessive sleepiness or sudden paroxysmal attacks of flaccid paralysis with conservation of consciousness), has been reported in several equine breeds, particularly Shetland ponies. The animal is otherwise healthy. During narcoleptic episodes, rapid eye movements occur, and at the same time, the animal may also show cataplexy or sudden loss of muscle tone with collapse.

Small Animals

Hydrocephalus is most common in dogs, particularly in toy and brachycephalic breeds. It can be classified as communicating (nonobstructive), in which CSF can flow freely into the subarachnoid space, or noncommunicating (obstructive). Known causes of noncommunicating hydrocephalus include atresia of the mesencephalic aqueduct, perinatal encephalitis, or adhesions caused by intraventricular hemorrhage at birth.

Clinical signs of hydrocephalus usually indicate cerebral dysfunction and often progress, although some animals may remain asymptomatic. The fontanelles are often patent, and affected animals may have ventrolateral strabismus. Blindness due to polymicrogyria (excessive number of smaller gyri) and asymmetric dilatations of the lateral ventricles have been described in Standard Poodles. Hydrocephalus has been observed in Saint Bernard puppies in association with aphakia (absence of the lens) and multiple ocular defects.

Imaging by ultrasonography (through the fontanelle), CT, or MRI can provide the diagnosis, and CSF analysis should identify encephalitis. In experimental models, aquaporin-4 and IL-6 are increased in dogs with idiopathic communicating internal hydrocephalus. Treatment relies on omeprazole (0.7 mg/kg, PO, once daily) to reduce CSF production or, if necessary, corticosteroids, or surgery to shunt CSF into the peritoneum.

Lissencephaly, an absence or reduction of cerebral gyri, is a rare disorder seen in Lhasa Apsos, Pekingese, and Australian Kelpies. It is also seen in association with cerebellar hypoplasia in Irish Setters, Wirehaired Fox Terriers, and Samoyeds and in Korat cats with microencephaly. Clinical signs consist of mild behavioral abnormalities and seizures.

Pug encephalitis is an ultimately fatal disease that may have a familial basis. There is some association with mutations on dog leukocyte antigen II loci in Pugs, Maltese, and Chihuahuas, as well as mutations in ILR7 and FBXW7. Affected Pugs show behavioral changes, seizures, and CSF pleocytosis. A similar nonsuppurative, necrotizing encephalitis has been reported in several other toy breed dogs, including Yorkshire Terriers, Chihuahuas, and Maltese Terriers.

Neonatal encephalopathy is an inherited genetic disorder caused by a mutation in the ATF-2 gene that has been described in Standard Poodles. Poodles appear stunted and weak from birth and begin seizuring at 4–5 weeks of age. The disease is fatal. A genetic test is available for diagnosis of this disease in Standard Poodles.

Polymicrogyria is an inherited disease identified in Standard Poodles that results in focal areas of the brain having smaller and more gyri than normal, resulting in disruption of function. The most common clinical signs are visual disturbances, but ataxia, behavioral problems, and hydrocephalus can also be seen. Clinical signs are attributable to the portion of the brain affected by the abnormal gyri.

Idiopathic epilepsy may be inherited in many breeds, including Beagles, Keeshonden, Irish Setters, Belgian Tervurens, Siberian Huskies, Springer Spaniels, Labrador Retrievers, Golden Retrievers, and German Shepherds. A mutation in CFA37 is suspected in Belgian Shepherds. Focal epilepsy of Lagotto Ramagnolo dogs is thought to be due to a mutation in Lgi2. A specific type of seizure known as temporal lobe epilepsy appears to be familial in Cavalier King Charles Spaniels and is characterized by behavioral manifestations such as "fly biting." The diagnosis of idiopathic epilepsy depends on eliminating other causes of seizures, particularly structural brain abnormalities (such as hydrocephalus or juvenile tumors), encephalitis, or metabolic causes (such as hepatic encephalopathy).

Paroxysmal dyskinesia is a type of movement disorder identified in several breeds of dogs, including the Softcoated Wheaten Terrier (for which a mutation in the PIGN gene has been identified), the Cavalier King Charles Spaniel (episodic falling; for which a mutation in the BCAN gene has been identified), Border Terrier (Spike's disease), and Chinook dog, among other pure and mixed breeds. Paroxysmal dyskinesias are episodes of involuntary movement including hyper- or hypotonicity or dysmetria and may resemble partial or generalized seizures, except that conscious awareness is maintained and no autonomic signs occur. Episodes may last minutes to hours and occur once over several months to multiple times daily.

Hepatic encephalopathy is usually caused by a congenital portosystemic shunt. The shunt may be a single large vessel, or there may be microscopic shunting of blood within the liver. Breeds often affected include Miniature Schnauzers, Yorkshire Terriers, Cairn Terriers, Australian Cattle Dogs, Old English Sheepdogs, and Maltese Terriers. The clinical signs are usually noticed before 6 months of age and primarily reflect cerebral dysfunction, including staring into space, inappropriate vocalizing, aggression, and agitation. Advanced neurologic alterations can cause depression, blindness, myoclonus, stupor, coma, or seizures. In cats, these signs are often accompanied by excessive salivation. A rare cause of hepatic encephalopathy is a deficiency of hepatic urea cycle enzymes.

Pre- and postprandial bile acid tests may support the diagnosis. Definitive diagnosis may be facilitated by use of radiographic imaging techniques, such as positive contrast portography, CT, transcolonic portal scintigraphy, or diagnostic gray-scale ultrasonography. Blood tests such as the ammonia tolerance test Ammonia: TSBA concentrations sensitively detect cholestatic disorders and conditions associated with portosystemic shunting. TSBA concentration should be measured before and 2 hr after meal ingestion... read more should be used with caution in cases of suspected hepatic encephalopathy because of risk of causing an encephalopathic crisis. Resting ammonia levels can be performed; however, ammonia levels have been poorly correlated with both the diagnosis and presence of clinical signs.

Lysosomal storage disorders that commonly cause cerebral signs include ceroid lipofuscinosis and fucosidosis, although there are many other forms of lysosomal storage disorders as well as other inborn errors of metabolism Congenital and InheritedMultifocal Disorders of the Nervous System in Animals Shaker calf syndrome is a neurodegenerative disorder that is seen in Hereford calves. Affected animals show a marked tremor within hours of birth, difficulty in rising, a stiff gait, and loss... read more . Genetic and enzymatic testing is available for many of these disorders. When specific tests are not available, organic acid screens may support the general diagnosis of metabolic error.

Puppy hypoglycemia is an idiopathic syndrome in toy breeds of dogs that is seen in the first 6 months of life. It seems to relate to a relative immaturity of the liver, which affects glycogenolysis and can usually be managed by providing frequent meals of a commercial puppy diet. The problem usually resolves as the puppy matures.

Narcolepsy or cataplexy is an autosomal-recessive inherited disorder in Doberman Pinschers, Labrador Retrievers, and Dachshunds and has been described in additional canine breeds. It is rare in cats. A mutation in the hypocretin (orexin) receptor 2 (Hcrtr2) gene has been identified in Doberman Pinschers. Attacks are often stimulated by excitement. It must be differentiated from various types of syncope. Physostigmine (0.025–0.1 mg/kg, IV) potentiates the frequency and severity of cataleptic attacks. Imipramine (0.5–1 mg/kg, PO, three times a day) can be used to control the severity of the cataplexy.

Others also read
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID

Test your knowledge

Neurologic conditions of horses
A horse is found stuck, lying down, with a halter on, in its stall with its feet up against a wall. The owner helps the horse to a standing position and then notices that the horse’s face is asymmetric. The lips and nostrils and eyelid on the same side are drooping. What is the most likely cause of this condition?
Become a Pro at using our website 

Also of Interest

Become a Pro at using our website 
TOP