Literature DB >> 9673904

Congenital myotonia in related kittens.

F H Hickford1, B R Jones, M A Gething, R Pack, M R Alley.   

Abstract

Four closely related domestic shorthair kittens were investigated following the detection of abnormalities in their gait, difficulty opening their mouths and muscle hypertrophy. They walked with a stiff, stilted gait, with the stiffness reducing during exercise. Startling of the kittens resulted in hyperextension of the limbs and falling to lateral recumbency, or spasm of the orbicularis oculi muscle, prolonged prolapse of the nictitating membranes and flattening of the ears. One kitten was intermittently dysphonic. Endotracheal intubation of the anaesthetised kittens was difficult due to an inability to open the mouth to a wide angle, and narrowing of the glottis due to muscle spasm. A diagnosis of congenital myotonia was made based on the clinical signs, the kittens' ages, typical myotonic discharges on electromyography, and the histopathological and histochemical findings in muscle. This is the first report of congenital myotonia in this species.

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Year:  1998        PMID: 9673904     DOI: 10.1111/j.1748-5827.1998.tb03651.x

Source DB:  PubMed          Journal:  J Small Anim Pract        ISSN: 0022-4510            Impact factor:   1.522


  2 in total

1.  A novel mutation in CLCN1 associated with feline myotonia congenita.

Authors:  Barbara Gandolfi; Rob J Daniel; Dennis P O'Brien; Ling T Guo; Melanie D Youngs; Stacey B Leach; Boyd R Jones; G Diane Shelton; Leslie A Lyons
Journal:  PLoS One       Date:  2014-10-30       Impact factor: 3.240

2.  A novel mutation of the CLCN1 gene in a cat with myotonia congenita: Diagnosis and treatment.

Authors:  Christian Woelfel; Kathryn Meurs; Steven Friedenberg; Nicole DeBruyne; Natasha J Olby
Journal:  J Vet Intern Med       Date:  2022-07-11       Impact factor: 3.175

  2 in total

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