Background Paramyotonia congenita and Brody disease are well-described conditions in humans, characterized by exercise-induced myotonic-like muscle stiffness. A syndrome similar to Brody disease has been reported in cattle. Reports of a similar syndrome in dogs are scarce. Objectives To define and describe the clinical, diagnostic, and genetic features and disease course of paradoxical pseudomyotonia in Spaniel dogs. Animals Seven client-owned dogs (4 English Springer Spaniels and 3 English Cocker Spaniels) with clinically confirmed episodes of exercise-induced generalized myotonic-like muscle stiffness. Methods Sequential case study. Results All dogs were <24 months of age at onset. The episodes of myotonic-like generalized muscle stiffnes...
Familial polymyositis in humans has predisposing genetic factors. Descriptions of breed-specific var...
Abstract: Congenital pseudo-myotonia (PMT) in Chianina cattle is a muscle function disorder which ...
A hereditary, non-inflammatory myopathy occurring in young great Danes with distinctive histological...
This report describes the clinical findings of a congenital pseudo-myotonia observed in ten genetica...
Paradoxical pseudomyotonia has previously been described in the English Cocker Spaniel (ECS) and Eng...
The authors present a muscle function disorder observed in 11 Chianina animals. The clinical pictur...
An inherited muscle disorder defined as \u201ccongenital pseudomyotonia\u201d has been described in ...
A Dutch Improved Red and White cross-breed heifer calf was evaluated for a muscular disorder resulti...
A Dutch Improved Red and White cross-breed heifer calf was evaluated for a muscular disorder resulti...
An inherited muscle disorder defined as \u201ccongenital pseudomyotonia\u201d has been described in ...
muscular stiffness in young labrador retrievers A novel movement disorder characterised by extreme g...
Objectives: To describe the clinical phenotype of a new motor disorder in Labrador Retrievers. Anima...
The clinical and clinicopathological characteristics, treatment and outcome of vermicular muscle con...
A congenital myopathy is reported in the only male puppy from a litter of Brittany Spaniels. The con...
Objectives: To describe the clinical phenotype of a new motor disorder in Labrador Retrievers. Anim...
Familial polymyositis in humans has predisposing genetic factors. Descriptions of breed-specific var...
Abstract: Congenital pseudo-myotonia (PMT) in Chianina cattle is a muscle function disorder which ...
A hereditary, non-inflammatory myopathy occurring in young great Danes with distinctive histological...
This report describes the clinical findings of a congenital pseudo-myotonia observed in ten genetica...
Paradoxical pseudomyotonia has previously been described in the English Cocker Spaniel (ECS) and Eng...
The authors present a muscle function disorder observed in 11 Chianina animals. The clinical pictur...
An inherited muscle disorder defined as \u201ccongenital pseudomyotonia\u201d has been described in ...
A Dutch Improved Red and White cross-breed heifer calf was evaluated for a muscular disorder resulti...
A Dutch Improved Red and White cross-breed heifer calf was evaluated for a muscular disorder resulti...
An inherited muscle disorder defined as \u201ccongenital pseudomyotonia\u201d has been described in ...
muscular stiffness in young labrador retrievers A novel movement disorder characterised by extreme g...
Objectives: To describe the clinical phenotype of a new motor disorder in Labrador Retrievers. Anima...
The clinical and clinicopathological characteristics, treatment and outcome of vermicular muscle con...
A congenital myopathy is reported in the only male puppy from a litter of Brittany Spaniels. The con...
Objectives: To describe the clinical phenotype of a new motor disorder in Labrador Retrievers. Anim...
Familial polymyositis in humans has predisposing genetic factors. Descriptions of breed-specific var...
Abstract: Congenital pseudo-myotonia (PMT) in Chianina cattle is a muscle function disorder which ...
A hereditary, non-inflammatory myopathy occurring in young great Danes with distinctive histological...