werdnig-hoffman disease Antonyms
No Synonyms and anytonyms found
Meaning of werdnig-hoffman disease
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
- 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.
- There is currently no cure for Werding-Hoffman disease, but treatments focus on managing symptoms and improving quality of life.
- Physical therapy, respiratory support, and nutritional management are essential components of care for patients with Werding-Hoffman disease.
- Genetic testing is crucial for diagnosing Werding-Hoffman disease and determining the prognosis.
- Research on gene therapy and other novel treatments offers hope for future advancements in the management of Werding-Hoffman disease.
- Support groups and advocacy organizations provide valuable resources for families affected by Werding-Hoffman disease.
- 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.
