Page 927 - Problem-Based Feline Medicine
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42 – THE WEAK AND ATAXIC OR PARALYZED CAT  919


           Pathogenesis                                        abnormal formation and/or protrusion of the
                                                               meninges and/or spinal cord.
           Spinal cord and vertebral anomalies are classified into
                                                             – Pathogenesis may involve initial failure of clo-
           abnormalities originating in the tissues of mesodermal
                                                               sure or the reopening of a previously closed neu-
           origin (vertebral body and intervertebral disc)  and
                                                               ral tube.
           those arising from tissues of ectodermal origin (spinal
                                                             – Spina bifida occulta represents an incomplete
           cord and meninges).
                                                               closure of one or more vertebral arches without
           Malformations of mesodermal origin.                 protrusion of meninges or spinal cord.
            ● Block vertebrae.                               – Spina bifida manifesta includes  meningocele
              – Caused by improper segmentation of somites,    (meningeal herniation through the vertebral arch
                resulting in stable vertebral fusion.          defect)  and meningomyelocele (herniation of
            ● Butterfly vertebrae.                             the spinal cord and meninges).
              – Abnormal  persistence of the  notochord (the  – The meningeal and/or spinal cord herniation may
                embryological precursor of intervertebral discs),  or may not communicate with the environment.
                producing a midline cranial to caudal cleft in the  ● Sacrococcygeal dysgenesis of Manx cats.
                vertebral body (when viewing the vertebra from  – An  autosomal semi-lethal dominant trait,
                the dorsoventral direction).                   providing the genetic basis for the absent tail
            ● Hemivertebrae.                                   as well as numerous vertebral and spinal cord
              – Produced by fusion of one lateral somite to one  abnormalities.
                on the contralateral side that is  not directly  – Homozygotes usually do not survive.
                opposed or by a lack of vascularization, lead-  – There are four phenotypic subgroups – a com-
                ing to a failure of ossification in part of the ver-  plete absence of coccygeal, sacral  +/− caudal
                tebral body. This produces a  wedge-shaped     lumbar vertebrae (the most severe); fused caudal
                vertebra, and scoliosis, lordosis or kyphosis.  vertebrae; mobile but kinked caudal vertebrae;
            ● Transitional vertebrae.                          and a normal tail.
              – Sacralization of the last lumbar vertebra is the
                most common in cats. In this condition, the last  Clinical signs
                lumbar vertebra has characteristics of both lum-
                bar vertebrae and the sacrum.             Clinical signs are dependent on the type of congenital
            ● Atlantoaxial subluxation.                   malformation and its location.
              – Results from hypoplasia or aplasia of the dens
                                                          Block vertebrae are usually stable.
                with secondary atlantoaxial instability.
                                                          ● Occasionally they can be stenotic or angulated,
              – It is either caused by a developmental failure
                                                             causing extradural spinal cord compression.
                of dens ossification  or an  ischemic necrosis
                                                          ● Disc extrusion can occur at disc spaces immediately
                and partial resorption of the dens as a result of
                                                             cranial and caudal to the block vertebrae.
                trauma.
              – The cranial portion of the axis is displaced into  Butterfly vertebrae are generally incidental findings.
                the spinal canal producing cord compression.
                                                          Hemivertebrae commonly lead to scoliosis, lordosis
           Malformations of ectodermal origin.            or kyphosis.
            ● Abnormalities of the vertebral arch and spinal cord  ● Signs are due to spinal cord compression or
              are primarily influenced by neural tube devel-  repeated trauma associated with vertebral instabil-
              opment.                                        ity. Instability produces osseous changes that sec-
            ● The most common anomaly is spina bifida.       ondarily compress the spinal cord.
            ● Spina bifida.                               ● Signs may be acute, chronic, progressive or inter-
              – The defects of spina bifida vary from  incom-  mittent, but are usually first noted within the first
                plete fusion of the vertebral arch to incom-  1–2 years of life.
                plete fusion of the neural tube, resulting in  ● Conformation may be visibly or palpably abnormal.
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