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Dejerine Sottas Disease synonyms

What other names are the Dejerine Sottas Disease known by? Synonyms and other terms with which Dejerine Sottas Disease is known.

Dejerine Sottas Disease is also known as...

Dejerine Sottas Disease Synonyms


Dejerine Sottas Disease, also known as Dejerine-Sottas neuropathy, is a rare genetic disorder that affects the peripheral nerves. It is named after the French neurologists Jules Dejerine and Pierre Marie Sottas, who first described the condition in the late 19th century.


This disease is characterized by the progressive degeneration of the peripheral nerves, which are responsible for transmitting signals between the brain and spinal cord to the rest of the body. As a result, individuals with Dejerine Sottas Disease experience muscle weakness, sensory loss, and impaired reflexes.


There are several synonyms used to refer to this condition:



  • Dejerine-Sottas neuropathy: This term highlights the neuropathic nature of the disease, emphasizing the damage to the peripheral nerves.

  • Hereditary motor and sensory neuropathy type III (HMSN III): This classification system categorizes Dejerine Sottas Disease as a subtype of hereditary motor and sensory neuropathy, which encompasses a group of genetic disorders affecting the peripheral nerves.

  • Charcot-Marie-Tooth disease type 3 (CMT3): Dejerine Sottas Disease is considered a severe form of Charcot-Marie-Tooth disease, a broader classification of inherited peripheral neuropathies.

  • Progressive hypertrophic neuropathy: This term emphasizes the progressive nature of the disease, as well as the characteristic hypertrophy (enlargement) of the peripheral nerves.


It is important to note that while these terms are used interchangeably, they all refer to the same underlying condition - Dejerine Sottas Disease. The choice of terminology may vary depending on the medical professional or the specific context in which the disease is being discussed.


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