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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 accompani...

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Autores principales: Kisipan, Mosiany L., Nyaga, Samuel N., Thuo, Jesse N., Nyakego, Phillip O., Orenge, Caleb O., Ojoo, Rodi O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397892/
https://www.ncbi.nlm.nih.gov/pubmed/31972069
http://dx.doi.org/10.1002/vms3.244
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author Kisipan, Mosiany L.
Nyaga, Samuel N.
Thuo, Jesse N.
Nyakego, Phillip O.
Orenge, Caleb O.
Ojoo, Rodi O.
author_facet Kisipan, Mosiany L.
Nyaga, Samuel N.
Thuo, Jesse N.
Nyakego, Phillip O.
Orenge, Caleb O.
Ojoo, Rodi O.
author_sort Kisipan, Mosiany L.
collection PubMed
description 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.
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spelling pubmed-73978922020-08-06 Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report Kisipan, Mosiany L. Nyaga, Samuel N. Thuo, Jesse N. Nyakego, Phillip O. Orenge, Caleb O. Ojoo, Rodi O. Vet Med Sci 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 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. John Wiley and Sons Inc. 2020-01-23 /pmc/articles/PMC7397892/ /pubmed/31972069 http://dx.doi.org/10.1002/vms3.244 Text en © 2020 The Authors. Veterinary Medicine and Science Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Report
Kisipan, Mosiany L.
Nyaga, Samuel N.
Thuo, Jesse N.
Nyakego, Phillip O.
Orenge, Caleb O.
Ojoo, Rodi O.
Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title_full Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title_fullStr Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title_full_unstemmed Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title_short Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report
title_sort lobar holoprosencephaly with craniofacial defects in a friesian calf: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397892/
https://www.ncbi.nlm.nih.gov/pubmed/31972069
http://dx.doi.org/10.1002/vms3.244
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