How Do You Spell AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY?

Pronunciation: [ˌɔːtə͡ʊsˈə͡ʊmə͡l ɹɪsˈɛsɪv pˌɒlɪsˈɪstɪk kˈɪdnɪ] (IPA)

The spelling of the word "Autosomal Recessive Polycystic Kidney" can be a bit daunting at first glance. However, using the International Phonetic Alphabet (IPA) can help make sense of it. The word is pronounced /ɔːtəsəʊməl rɪˈsɛsɪv pɒlɪˈsɪstɪk ˈkɪdni/, with emphasis on the second syllable of each word. The term refers to a genetic disorder that affects the kidneys, causing the growth of numerous cysts. While the spelling may be complex, awareness and understanding of the condition can help those affected seek proper treatment.

AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY Meaning and Definition

  1. Autosomal Recessive Polycystic Kidney (ARPKD) is a rare, genetic disorder characterized by the development of multiple fluid-filled cysts in the kidneys. It is referred to as "autosomal recessive" as the condition occurs due to mutations in both copies of a specific gene, and both parents must be carriers of the gene mutation for the child to be affected.

    The primary manifestation of ARPKD is the enlargement of the kidneys due to the formation of countless cysts within the organ. These cysts can impair kidney function, leading to complications such as high blood pressure, urinary tract infections, kidney stones, and renal failure. In some cases, the liver may also be affected, with cysts developing in this organ as well.

    ARPKD typically presents in infancy or early childhood. Its symptoms may include abdominal swelling, difficulty feeding, frequent urination, blood in urine, and occasionally, high blood pressure. Due to the severity and potential complications associated with ARPKD, early diagnosis and management are crucial for improved long-term outcomes.

    Treatment for ARPKD primarily focuses on addressing the associated complications and providing supportive care. Depending on the individual's specific needs, interventions may involve medication to control blood pressure, dietary modifications to manage kidney function, dialysis in cases of renal failure, or ultimately, kidney transplantation.

    Overall, Autosomal Recessive Polycystic Kidney is a genetic disorder characterized by the development of multiple cysts in the kidneys, leading to kidney dysfunction and potential liver involvement.

Common Misspellings for AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY

  • zutosomal recessive polycystic kidney
  • sutosomal recessive polycystic kidney
  • wutosomal recessive polycystic kidney
  • qutosomal recessive polycystic kidney
  • aytosomal recessive polycystic kidney
  • ahtosomal recessive polycystic kidney
  • ajtosomal recessive polycystic kidney
  • aitosomal recessive polycystic kidney
  • a8tosomal recessive polycystic kidney
  • a7tosomal recessive polycystic kidney
  • aurosomal recessive polycystic kidney
  • aufosomal recessive polycystic kidney
  • augosomal recessive polycystic kidney
  • auyosomal recessive polycystic kidney
  • au6osomal recessive polycystic kidney
  • au5osomal recessive polycystic kidney
  • autisomal recessive polycystic kidney
  • autksomal recessive polycystic kidney
  • autlsomal recessive polycystic kidney
  • autpsomal recessive polycystic kidney

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