Difference between revisions of "Muscles Developmental - Pathology"

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*Clefts may lead to [[Hernia, Pleuroperitoneal Diaphragmatic|herniation]] of abdominal organs into thoracic cavity in any species
 
*Clefts may lead to [[Hernia, Pleuroperitoneal Diaphragmatic|herniation]] of abdominal organs into thoracic cavity in any species
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*Unknown cause
 
*Unknown cause
 
*Responsible for significant deaths
 
*Responsible for significant deaths
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**Increased number of myofibres in affected muscle (thighs, rump, loin)
 
**Increased number of myofibres in affected muscle (thighs, rump, loin)
 
**Predisposes to dystocia
 
**Predisposes to dystocia
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*Inadequate [[Muscle Regeneration - Anatomy & Physiology|regeneration]], [[Muscles Hyperplastic and Neoplastic - Pathology#Hypertrophy|compensatory hypertrophy]]
 
*Inadequate [[Muscle Regeneration - Anatomy & Physiology|regeneration]], [[Muscles Hyperplastic and Neoplastic - Pathology#Hypertrophy|compensatory hypertrophy]]
 
*More about [[Muscular dystrophy]]
 
*More about [[Muscular dystrophy]]
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**Causes [[Hypertrophic Cardiomyopathy|hypertrophic cardiomyopathy]] and hepatomegaly
 
**Causes [[Hypertrophic Cardiomyopathy|hypertrophic cardiomyopathy]] and hepatomegaly
 
**Glycogen in skeletal and cardiac muscle, neurons nad hepatocytes
 
**Glycogen in skeletal and cardiac muscle, neurons nad hepatocytes
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*No clinical significance
 
*No clinical significance
 
*Noticed at slaughter or necropsy
 
*Noticed at slaughter or necropsy
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**Non-specific muscle [[Muscles Degenerative - Pathology#Atrophy|disuse atrophy]] and fibrosis or no changes on histology
 
**Non-specific muscle [[Muscles Degenerative - Pathology#Atrophy|disuse atrophy]] and fibrosis or no changes on histology
 
*Both forms manifest as weakness which worsens on exercise
 
*Both forms manifest as weakness which worsens on exercise
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[[Category:Muscles - Developmental Pathology]]
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===[[Canine Dermatomyositis]]===
 
===[[Canine Dermatomyositis]]===

Revision as of 17:23, 3 March 2011

Congenital diaphragmatic defects

  • Clefts may lead to herniation of abdominal organs into thoracic cavity in any species


Myofibrillar hypoplasia

  • In piglets
  • = Splayleg
  • May spontaneously resolve
  • Unknown cause
  • Responsible for significant deaths


Hyperplasia of muscle fibres

  • In calves and lambs
  • “Double muscling”
    • Increased number of myofibres in affected muscle (thighs, rump, loin)
    • Predisposes to dystocia


Muscular dystrophies

  • Inherited group of degenerative muscular diseases
  • Progressive muscle weakness and wasting
  • Usually due to a genetic fault -> muscular protein deficiency
    • Duchenne MD in humans due to dystrophin deficiency also present in some animals
    • Dystrophin gene mutations reported in the Golden Retriever, Rottweiler, German shorthaired pointer and Irish terrier etc.
  • Inadequate regeneration, compensatory hypertrophy
  • More about Muscular dystrophy


Glycogen storage diseases

  • Caused by a deficiency of an enzyme
  • See general pathology
  • Type II glycogenosis
    • Deficiency of acid maltase
    • In Shorthorn cattle
    • Muscular weakness and incoordination
    • Glycogen stored in skeletal muscle, heart and CNS
    • Type I and II muscle fibres contain glycogen vacuoles
  • Type III glycogenosis
    • Deficiency of debranching enzyme
    • In dogs
    • Causes hypertrophic cardiomyopathy and hepatomegaly
    • Glycogen in skeletal and cardiac muscle, neurons nad hepatocytes


Steatosis

  • Also called lipomatosis
  • In cattle, sheep and pigs
  • Fat replaces lost muscle fibres
  • Pale muscle, bilaterally symmetrical
  • No clinical significance
  • Noticed at slaughter or necropsy


Myasthenia gravis (MG)

  • Acquired
    • Autoimmune disease
      • Antibodies directed against acetyl choline receptors
    • Associated with thymomas, megaoesophagus and dysphagia
    • In adult dogs
  • Congenital
    • Inherited deficiency in acetyl choline receptors
    • Rare
    • Newfoundland, Jack Russel Terrier, Springer Spaniels – genetic predisposition
    • In dogs – 4 DLA genes recognized: DLA-12, DLA-88, DLA-79 and DLA-64
    • Associated with HLA gene in humans
    • No antibodies against acetyl choline receptors in serum
    • Non-specific muscle disuse atrophy and fibrosis or no changes on histology
  • Both forms manifest as weakness which worsens on exercise


Canine Dermatomyositis

Porcine stress syndrome