werdnig-hoffman disease Synonyms

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werdnig-hoffman disease Meaning

Wordnet

werdnig-hoffman disease (n)

autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; death usually occurs in early childhood

werdnig-hoffman disease Sentence Examples

  1. Werding-Hoffman disease, also known as Spinal Muscular Atrophy, is a genetic disorder characterized by progressive muscle weakness and atrophy.
  2. Symptoms of Werding-Hoffman disease typically manifest in infancy, with difficulty breathing, feeding, and motor control.
  3. The severity of Werding-Hoffman disease varies greatly, with some patients experiencing rapid progression to respiratory failure, while others exhibit a more gradual decline.
  4. The underlying cause of Werding-Hoffman disease is a mutation in the SMN1 gene, which leads to a deficiency of the survival motor neuron protein.
  5. There is currently no cure for Werding-Hoffman disease, but treatments focus on managing symptoms and improving quality of life.
  6. Physical therapy, respiratory support, and nutritional management are essential components of care for patients with Werding-Hoffman disease.
  7. Genetic testing is crucial for diagnosing Werding-Hoffman disease and determining the prognosis.
  8. Research on gene therapy and other novel treatments offers hope for future advancements in the management of Werding-Hoffman disease.
  9. Support groups and advocacy organizations provide valuable resources for families affected by Werding-Hoffman disease.
  10. Early diagnosis and intervention are essential for optimizing outcomes and improving the well-being of patients with Werding-Hoffman disease.

FAQs About the word werdnig-hoffman disease

autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; de

No synonyms found.

No antonyms found.

Werding-Hoffman disease, also known as Spinal Muscular Atrophy, is a genetic disorder characterized by progressive muscle weakness and atrophy.

Symptoms of Werding-Hoffman disease typically manifest in infancy, with difficulty breathing, feeding, and motor control.

The severity of Werding-Hoffman disease varies greatly, with some patients experiencing rapid progression to respiratory failure, while others exhibit a more gradual decline.

The underlying cause of Werding-Hoffman disease is a mutation in the SMN1 gene, which leads to a deficiency of the survival motor neuron protein.