What does CIPA mean in HUMAN GENOME
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare and serious neurodevelopmental disorder that affects the body's ability to perceive physical pain and thermoregulation. People with CIPA lack the ability to feel pain, temperature, and itch. They also experience anhidrosis, which is absence of sweating.
CIPA meaning in Human Genome in Medical
CIPA mostly used in an acronym Human Genome in Category Medical that means Congenital insensitivity to pain with anhidrosis
Shorthand: CIPA,
Full Form: Congenital insensitivity to pain with anhidrosis
For more information of "Congenital insensitivity to pain with anhidrosis", see the section below.
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Essential Questions and Answers on Congenital insensitivity to pain with anhidrosis in "MEDICAL»GENOME"
What are the main symptoms of CIPA?
The main symptoms of CIPA include inability to feel pain, temperature, or itching; anhidrosis; chronic infections; joint contractures; fractures; and ulcers caused by repetitive trauma.
How does CIPA affect thermoregulation?
People with CIPA experience anhidrosis, which means they cannot sweat. This can cause difficulty regulating body temperature and increase the risk of hyperthermia or heat stroke in hot environments.
Who is at risk for developing CIPA?
CIPA is a genetic disorder that is passed down in families through autosomal recessive inheritance, where both parents must be carriers of the gene for their child be affected by CIPA.
Final Words:
Although there is no cure for Congenital Insensitivity to Pain with Anhidrosis (CIPA), early diagnosis and management can help minimize complications and improve quality of life for those affected by this condition. Through genetic testing, physical exams, skin biopsies, and neurological testing, doctors can accurately diagnose this condition so people have access to necessary treatments and interventions.
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