How Do You Spell AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA HEREDITARY?

Pronunciation: [ˌɔːtə͡ʊsˈə͡ʊmə͡l dˈɒmɪnənt spˈastɪk pˌaɹəplˈiːd͡ʒə hɪɹˈɛdɪtəɹi] (IPA)

Autosomal Dominant Spastic Paraplegia Hereditary is a genetic disorder that affects the nervous system. The spelling of this word can be explained using IPA phonetic transcription. The first word "Autosomal" is pronounced as /ˌɔːtəˈsəʊməl/. The next word, "Dominant", is pronounced as /ˈdɒmɪnənt/. The third word, "Spastic", is pronounced as /ˈspæstɪk/. The fourth word, "Paraplegia", is pronounced as /ˌpærəˈpliːdʒə/. The final word, "Hereditary", is pronounced as /həˈrɛdɪtəri/. Overall, this complex spelling emphasizes the intricate and specialized nature of genetics and biology.

Meaning and Definition
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AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA HEREDITARY Meaning and Definition

  1. Autosomal Dominant Spastic Paraplegia Hereditary (ADSPH) is a genetic disorder characterized by the progressive degeneration of the nerves that control voluntary movement in the lower limbs. The term "autosomal" refers to the fact that the disease is inherited through a non-sex chromosome, meaning it can affect both males and females equally. "Dominant" indicates that a person needs to inherit only one copy of the defective gene from either parent to develop the condition, as opposed to "recessive" conditions that require two copies of the gene.

    The primary symptom of ADSPH is spastic paraplegia, which refers to stiffness and weakness in the legs due to the degeneration of nerve pathways controlling muscle movement. This typically leads to difficulties in walking and a progressive impairment of mobility. Other common symptoms include muscle cramps, muscle spasms, bladder dysfunction, and reduced sensation in the limbs. The severity and rate of progression of the disease can vary among individuals with ADSPH.

    ADSPH is caused by mutations in different genes, with several subtypes identified based on the specific genetic abnormality. These genes are involved in various cellular processes essential for nerve function and maintenance. The condition is usually diagnosed through a combination of physical examination, family history, and genetic testing.

    Currently, there is no cure for ADSPH. Treatment primarily focuses on reducing symptoms and improving quality of life. This may include physical therapy to manage spasticity and maintain muscle strength, assistive devices like orthotics or walking aids, and medications to alleviate muscle stiffness and pain. Genetic counseling is also recommended for affected individuals and their families to understand the inheritance pattern and the risk of passing it on to future generations.

Common Misspellings for AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA HEREDITARY

  • zutosomal dominant spastic paraplegia hereditary
  • sutosomal dominant spastic paraplegia hereditary
  • wutosomal dominant spastic paraplegia hereditary
  • qutosomal dominant spastic paraplegia hereditary
  • aytosomal dominant spastic paraplegia hereditary
  • ahtosomal dominant spastic paraplegia hereditary
  • ajtosomal dominant spastic paraplegia hereditary
  • aitosomal dominant spastic paraplegia hereditary
  • a8tosomal dominant spastic paraplegia hereditary
  • a7tosomal dominant spastic paraplegia hereditary
  • aurosomal dominant spastic paraplegia hereditary
  • aufosomal dominant spastic paraplegia hereditary
  • augosomal dominant spastic paraplegia hereditary
  • auyosomal dominant spastic paraplegia hereditary
  • au6osomal dominant spastic paraplegia hereditary
  • au5osomal dominant spastic paraplegia hereditary
  • autisomal dominant spastic paraplegia hereditary
  • autksomal dominant spastic paraplegia hereditary
  • autlsomal dominant spastic paraplegia hereditary
  • autpsomal dominant spastic paraplegia hereditary

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Correct spelling for Autosomal Dominant Spastic Paraplegia Hereditary
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