What does INAD mean in NEUROLOGY


Infantile neuroaxonal dystrophy (INAD) is an inherited disorder of the nervous system. It is characterized by progressive deterioration of nerve cells leading to impaired movement, delayed development, and other neurological problems.

INAD

INAD meaning in Neurology in Medical

INAD mostly used in an acronym Neurology in Category Medical that means Infantile neuroaxonal dystrophy

Shorthand: INAD,
Full Form: Infantile neuroaxonal dystrophy

For more information of "Infantile neuroaxonal dystrophy", see the section below.

» Medical » Neurology

Essential Questions and Answers on Infantile neuroaxonal dystrophy in "MEDICAL»NEUROLOGY"

What causes INAD?

INAD is caused by a defect in the PLA2G6 gene that leads to abnormal accumulation of fatty substances in the brain. This can lead to damage and death of the nerve cells over time.

What are the symptoms of INAD?

Symptoms of INAD can vary from person to person but often include developmental delays, dementia, difficulty walking, spasticity, seizures, vision problems, and hypotonia.

How is INAD diagnosed?

INAD is typically diagnosed through genetic testing and a physical examination. Additional tests such as MRI or CT scans may be used to confirm diagnosis and monitor progression of symptoms.

Is there any treatment for INAD?

Unfortunately there is no cure for INAD at this time; however there are treatments available which can help manage symptoms. These treatments focus on improving motor skills, language development, cognitive function, social functioning and physical therapy.

Can INAD affect life expectancy?

The severity of symptoms can vary from person to person but in general life expectancy for someone with INAD tends to be shorter than average due to the progressive nature of the disease. However early diagnosis and intervention can help improve quality of life for those affected by this condition.

Final Words:
Infantile neuroaxonal dystrophy (INAD) is a rare inherited condition that affects both physical and mental health and has no known cure. Early detection and appropriate interventions can help patients manage their symptoms while improving their overall quality of life.

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