Literature DB >> 23676552

Phenotypic characteristics of hydrocephalus in stillborn Friesian foals.

K D Sipma1, P Cornillie, M N Saulez, T A E Stout, G Voorhout, W Back.   

Abstract

Hydrocephalus is uncommon in horses. However, in recent years, it has become clear that the prevalence of hydrocephalus is greater in Friesian horses than in other breeds probably due to their limited gene pool. Before identification of candidate genes that predispose to the development of hydrocephalus in Friesian horses can be pursued, an in-depth, phenotypic, pathological description of the condition in Friesians would be of great benefit. Our study aimed to characterize the morphology of hydrocephalus in Friesian horses, to support further investigation of the genetic background of this condition. Four stillborn Friesian foals with hydrocephalus were examined macroscopically and microscopically and compared with 2 normal stillborn Friesian foals without hydrocephalus. In all clinical cases, tetraventricular and venous dilatations were observed, together with malformation of the petrosal bone and, as a result, narrowing of the jugular foramen. These observations suggest a communicative hydrocephalus with a diminished absorption of cerebrospinal fluid into the systemic circulation at the venous sinuses due to a distorted, nonfunctional jugular foramen. This type of hydrocephalus is also recognized in humans and dogs and has been linked genetically to chondrodysplasia; this has already been recognized in dwarfism, which is another monogenetic defect in Friesian horses.

Entities:  

Keywords:  horse; hydrocephalus; jugular foramen; phenotype; stillbirth

Mesh:

Year:  2013        PMID: 23676552     DOI: 10.1177/0300985813488955

Source DB:  PubMed          Journal:  Vet Pathol        ISSN: 0300-9858            Impact factor:   2.221


  3 in total

1.  Congenital hydrocephalus in a Belgian draft horse associated with a nonsense mutation in B3GALNT2.

Authors:  David Scott Kolb; Claudia Klein
Journal:  Can Vet J       Date:  2019-02       Impact factor: 1.008

2.  Whole genome sequencing identified a 16 kilobase deletion on ECA13 associated with distichiasis in Friesian horses.

Authors:  E A Hisey; H Hermans; Z T Lounsberry; F Avila; R A Grahn; K E Knickelbein; S A Duward-Akhurst; M E McCue; T S Kalbfleisch; M E Lassaline; W Back; R R Bellone
Journal:  BMC Genomics       Date:  2020-11-30       Impact factor: 3.969

3.  A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses.

Authors:  Bart J Ducro; Anouk Schurink; John W M Bastiaansen; Iris J M Boegheim; Frank G van Steenbeek; Manon Vos-Loohuis; Isaac J Nijman; Glen R Monroe; Ids Hellinga; Bert W Dibbits; Willem Back; Peter A J Leegwater
Journal:  BMC Genomics       Date:  2015-10-09       Impact factor: 3.969

  3 in total

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