Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
Background Holoprosencephaly is a forebrain deformity that results from varying degrees of separation failure of cerebral hemispheres. The condition is classified based on the degree of non‐separation of the hemispheres which, in turn, determines its severity. Holoprosencephaly is usually accompanie...
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Published in | Veterinary medicine and science Vol. 6; no. 3; pp. 454 - 461 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.08.2020
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Holoprosencephaly is a forebrain deformity that results from varying degrees of separation failure of cerebral hemispheres. The condition is classified based on the degree of non‐separation of the hemispheres which, in turn, determines its severity. Holoprosencephaly is usually accompanied by craniofacial defects whose severity tends to reflect the extent of brain deformities. In humans, holoprosencephaly is one of the commonest congenital brain anomalies but in animals, reported cases are scarce. The condition has multifactorial aetiology that involves interactions between several genetic and environmental factors.
Case presentation
A 4‐day‐old female Friesian calf with a deformed face was reported to the Faculty of veterinary medicine and surgery, Egerton University. The calf and the dam were sired by the same bull. On clinical and radiographic examination, the calf had a short snout that curved dorsally with bilateral cleft lip, right‐sided cleft jaw and a largely absent primary palate. Anatomopathological examination revealed brain deformities which included ventral fusion of frontal lobes of cerebral hemispheres, large merged lateral ventricles without septum pellucidum and fornix, hypoplastic corpus callosum, high degree of non‐separation between diencephalic structures, poorly developed hippocampal formation and hypoplastic olfactory lobe, optic chiasma, and nerve.
Conclusion
The case was confirmed as lobar holoprosencephaly based on characteristic anatomopathological findings. The aetiology of the defects in the present case could not be determined though they are thought to be either a result of recessive inheritance or exposure to teratogenic steroid alkaloids through materials fed to the dam during early pregnancy.
HPE is a spectrum of brain deformities often accompanied by CFDs that results from varying degrees of non‐separation of cerebral hemispheres. A 4‐day old calf with OFCs was examined and then euthanized on animal welfare grounds followed by anatomopathological findings that revealed brain deformities characteristic of HPE such as ventral fusion of frontal lobes, merged lateral ventricles and hypoplastic corpus callosum among others. The aetiology of the deformity in the current case could not be determined but thought to have probably resulted from recessive inheritance or exposure of teratogenic steroid alkaloid from dam's feed material during early pregnancy. |
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Bibliography: | Information Funding The authors declare that they did not receive any funding to conduct this study. Funding Information |
ISSN: | 2053-1095 2053-1095 |
DOI: | 10.1002/vms3.244 |