Bill

Bill > AJR104


NJ AJR104

NJ AJR104
Designates October 23 of each year as "Aromatic L-amino Acid Decarboxylase Deficiency Awareness Day."


summary

Introduced
02/01/2024
In Committee
02/01/2024
Crossed Over
Passed
Dead
01/12/2026

Introduced Session

2024-2025 Regular Session

Bill Summary

This resolution establishes October 23 of each year as "Aromatic L-Amino Acid Decarboxylase Deficiency Day" in New Jersey. The State of New Jersey supports protecting the health of vulnerable populations and young children, as well as educating the public and medical communities about rare diseases. A rare disease is generally considered to be a disease that affects fewer than 200,000 people in the United States at any given time. Aromatic L-Amino Acid Decarboxylase ("AADC") Deficiency is a life-limiting, severely debilitating genetic neurologic rare disease that significantly impacts a patient's development, motor skills, growth, cognition, and language skills. While some patients who are born with AADC Deficiency may be asymptomatic at birth, AADC patients typically experience symptoms within the first year of life such as developmental delay and involuntary eye movements. Caregivers of patients with AADC Deficiency are often responsible for the overall care of the patient due to the debilitating nature of this disease and patients may need life-long care. The State of New Jersey can raise awareness of AADC Deficiency in the public and medical communities within this State in order to support individuals with AADC Deficiency and their caregivers by designating this awareness day.

AI Summary

This joint resolution designates October 23 of each year as "Aromatic L-amino Acid Decarboxylase Deficiency Awareness Day" in New Jersey, aiming to raise public understanding of this rare genetic neurological disorder. AADC Deficiency is a severe condition affecting approximately 1 in 100,000 people, characterized by a lack of the AADC enzyme necessary for producing dopamine, which prevents patients from developing critical motor skills, communication abilities, and basic life functions. The resolution recognizes that patients typically experience symptoms within the first year of life, such as developmental delays and involuntary eye movements, and that caregivers often provide lifelong care due to the disease's debilitating nature. The Governor is respectfully requested to issue an annual proclamation and encourage public officials, private organizations, and citizens to observe the day with appropriate awareness activities and programs, ultimately supporting individuals with AADC Deficiency and their caregivers by increasing public and medical community understanding of this rare condition.

Committee Categories

Health and Social Services

Sponsors (1)

Last Action

Introduced, Referred to Assembly Health Committee (on 02/01/2024)

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