nutritional myopathy - meaning and definition. What is nutritional myopathy
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What (who) is nutritional myopathy - definition

MYOPATHY CHARACTERIZED BY ABNORMALLY LOCATED NUCLEI IN SKELETAL MUSCLE CELLS
Centronuclear myopathy (including myotubular myopathy); Centronuclear myopathy, congenital; Congenital centronuclear myopathy

Nutritional muscular dystrophy         
  • Typical stance of affected lambs, with arched back
DISEASE CAUSED BY A DEFICIENCY OF SELENIUM AND VITAMIN E IN DIETARY INTAKE
White muscle disease; Nutritional myopathy; Nutritional Myopathy
Nutritional Muscular Dystrophy (Nutritional Myopathy or White Muscle Disease) is a disease caused by a deficiency of selenium and vitamin E in dietary intake. Soils that contains low levels of selenium produce forages and grains that are deficient in selenium.
Centronuclear myopathy         
Centronuclear myopathies (CNM) are a group of congenital myopathies where cell nuclei are abnormally located in the center of muscle cells instead of their normal location at the periphery.
Nemaline myopathy         
  • An example of muscle cells with rods. The rods have been stained red and are located on the inside of the plasma membrane.
  • Example of a sarcomere with nemaline rods.
  • This is a simple example of a healthy sarcomere.
CONGENITAL STRUCTURAL MYOPATHY CHARACTERIZED BY GENERALLY NON-PROGRESSIVE MUSCLE WEAKNESS OF VARYING SEVERITY
Nemaline Myopathy; Rod myopathy; Myopathies, nemaline; Nemaline body disease; Nemaline rod myopathy; Nemaline Myopathy, Amish Type; Amish nemaline myopathy; Nemaline myopathy, Amish type
Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, often hereditary neuromuscular disorder with many symptoms that can occur such as muscle weakness, hypoventilation, swallowing dysfunction, and impaired speech ability. The severity of these symptoms varies and can change throughout one's life to some extent.

Wikipedia

Centronuclear myopathy

Centronuclear myopathies (CNM) are a group of congenital myopathies where cell nuclei are abnormally located in the center of muscle cells instead of their normal location at the periphery.

Symptoms of CNM include severe hypotonia, hypoxia-requiring breathing assistance, and scaphocephaly. Among centronuclear myopathies, the X-linked myotubular myopathy form typically presents at birth, and is thus considered a congenital myopathy. However, some centronuclear myopathies may present later in life.