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Muscular Dystrophy
Ullrich-like
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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​Muscular dystrophies are examples of degenerative myopathic conditions of both dogs and cats. Ullrich-like muscular dystrophy is a type of congenital muscular disorder characterized by muscle weakness, joint contracture, and hyperlaxity.
Age of Onset: 6-7 months of age
​
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over the course of a few months
​
Clinical Signs:
​Posture and Appearance
Multifocal joint contracture
Thickening of elbow and stifle joints
Distal limb joint hyperlaxity
Low head carriage
​Moderate lumbar and thoracic kyphosis

Movement
Severe generalized weakness
Difficulty rising and ambulating
Ambulatory tetraparesis ("stiff, choppy, short-strided gait")

Spinal Reflexes
Reduced withdrawal reflexes

Painful Reactions
Mild spinal hyperesthesia

Muscle Atrophy
Generalized muscle atrophy
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Diffuse neuromuscular
​
Unknown
​To read more about this disease click below:
References
X-Linked
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Muscular dystrophies are examples of degenerative myopathic conditions of both dogs and cats. These diseases are exemplified by an X-linked disease of golden retrievers and other breeds. In humans, this type of muscular dystrophy is referred to as Duchenne's muscular dystrophy.  These disease processes result from gene-associated abnormalities of a muscle membrane protein (dystrophin).
Age of Onset: 6-9 weeks of age
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Sex Predisposition: Males are more commonly affected
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Clinical Course:
​Clinical signs may plateau after 6 months of progressive deterioration.
​

Clinical Signs:
Posture and Appearance
Plantigrade stance
Kyphosis to lordosis

Movement
Weakness
“Stiffness”
“Shuffling” gait
Abduction of elbows
Bunny-hopping gait
Exercise-intolerance


Cranial Nerves
Enlargement of the base of the tongue
Inability to fully open the jaw
Weak barking/dysphonia

Special Functions (e.g. respiration; urination)
Salivation
Pharyngeal and esophageal dysfunction

Muscle Atrophy
Generalized muscle atrophy (head and limb muscles)
Generalized muscle hypertrophy
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Diffuse neuromuscular disease
X-linked recessive mutation in dystrophin gene
​To read more about this disease click below:
References
To read more about this disease click below:
References
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