How Do You Spell CONGENITAL HYPOCUPREMIA?

Pronunciation: [kənd͡ʒˈɛnɪtə͡l hˌa͡ɪpə͡ʊkʌpɹˈiːmi͡ə] (IPA)

Congenital Hypocupremia is a genetic disorder characterized by low levels of copper in the blood. The spelling of this medical term may appear complex, but it can be easily explained using the International Phonetic Alphabet (IPA). The word consists of three syllables: con-gen-i-tal hy-po-cu-pre-mi-a, with stress on the second syllable. The "c" in "cu" is pronounced as "k", the "pre" in "premia" is pronounced as "pree". The correct spelling and pronunciation of medical terms are essential for effective communication between healthcare professionals and patients.

CONGENITAL HYPOCUPREMIA Meaning and Definition

1. Congenital hypocupremia is a rare genetic disorder characterized by a deficiency of copper in the body from birth. Copper is an essential mineral that plays a crucial role in various bodily functions, including the production of red blood cells, maintenance of the nervous system, and formation of connective tissues. In individuals with congenital hypocupremia, there is a defect in the transport or absorption of copper, leading to abnormally low levels of this mineral in the body.

   Symptoms of congenital hypocupremia can vary, but commonly include anemia, developmental delays, failure to thrive, and neurological abnormalities. These neurological abnormalities may present as movement disorders, muscle weakness, or impaired coordination. Copper deficiency can also affect the functioning of the cardiovascular system, causing abnormal heart rhythms or other cardiovascular complications.

   Due to the early onset of this condition, it is often detected in infancy or early childhood. Diagnosis is typically confirmed through blood tests that measure copper levels or identify specific genetic mutations associated with congenital hypocupremia.

   Treatment for congenital hypocupremia usually involves copper supplementation, often in the form of oral copper supplements or intravenous administration in severe cases. Regular monitoring of copper levels and careful management of copper supplementation is necessary to maintain appropriate levels in the body without causing toxicity.

   Overall, congenital hypocupremia is a rare genetic disorder characterized by copper deficiency from birth, leading to various physical, neurological, and cardiovascular complications. Early diagnosis and proper management are essential to prevent and manage symptoms associated with this condition.

Common Misspellings for CONGENITAL HYPOCUPREMIA

• xongenital hypocupremia
• vongenital hypocupremia
• fongenital hypocupremia
• dongenital hypocupremia
• cingenital hypocupremia
• ckngenital hypocupremia
• clngenital hypocupremia
• cpngenital hypocupremia
• c0ngenital hypocupremia
• c9ngenital hypocupremia
• cobgenital hypocupremia
• comgenital hypocupremia
• cojgenital hypocupremia
• cohgenital hypocupremia
• confenital hypocupremia
• convenital hypocupremia
• conbenital hypocupremia
• conhenital hypocupremia
• conyenital hypocupremia
• contenital hypocupremia

Etymology of CONGENITAL HYPOCUPREMIA

The word "Congenital Hypocupremia" has its etymology rooted in Latin and Greek.

The term "congenital" comes from the Latin word "congenitus", which means "born together" or "from birth". It indicates a condition or trait that is present from birth or that originates during fetal development.

"Hypocupremia" is composed of two Greek roots: "hypo" meaning "below" or "deficient", and "cuprum" which refers to copper in Latin. Copper is an essential trace element in the human body that plays a role in various biological processes.

Therefore, "Congenital Hypocupremia" can be broken down to mean a condition of deficient or below-normal levels of copper present from birth.