Evidence map›Paper›PMID 31972069›Full record

ArticleVeterinary medicine and science2020

Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report.

Mosiany L Kisipan, Samuel N Nyaga, Jesse N Thuo, Phillip O Nyakego, Caleb O Orenge, Rodi O Ojoo

Open access · goldAbstract readCase Reports
In one paragraph

Article in Veterinary medicine and science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Multiple Cephalic Malformations in a Calf.Animals : an open access journal from MDPI · 2020
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Mosiany L KisipanDepartment of Veterinary Anatomy and Physiology, Egerton University, Egerton, Kenya.ORCID 0000-0003-1653-611X
Samuel N NyagaDepartment of Veterinary Anatomy and Physiology, Egerton University, Egerton, Kenya.
Jesse N ThuoDepartment of Veterinary Anatomy and Physiology, Egerton University, Egerton, Kenya.
Phillip O NyakegoDepartment of Veterinary Anatomy and Physiology, Egerton University, Egerton, Kenya.
Caleb O OrengeDepartment of Veterinary Anatomy and Physiology, Egerton University, Egerton, Kenya.
Rodi O OjooDepartment of Veterinary Anatomy and Physiology, University of Nairobi, Nairobi, Kenya.
Egerton University · KEUniversity of Nairobi · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHoloprosencephaly 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.

conclusionThe 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.

Indexed as

AnimalsCattleCattle DiseasesFemaleHoloprosencephalyCongenital malformationcraniofacial defectsforebrainholoprosencephalyorofacial defects

Identifiers

PMID31972069
PMCPMC7397892
OpenAlexW3001485394

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.