HR 1652: Turner Syndrome Awareness Day; February 28, 2026; recognize
Last action March 9, 2026 · House Read and Adopted
A Georgia House resolution designates February 28, 2026, as Turner Syndrome Awareness Day, aiming to raise public awareness about the chromosomal disorder and its health risks.
The summaries below were written by an AI model (claude-sonnet-5) from the text of the resolution and are not part of it. Quote the text, not the summary. The stored text is the Introduced version, the latest LegiScan holds.
In plain language
This resolution from the Georgia House of Representatives recognizes February 28, 2026, as Turner Syndrome Awareness Day. It does not change any Georgia law; instead it is a formal statement from the House explaining what Turner Syndrome is, noting it affects about one in every 2,500 live female births, and highlighting risks such as learning difficulties, growth failure, hearing problems, and a greatly increased risk of aortic dissection, a life-threatening tear in the aorta. The resolution notes that funding for Turner Syndrome research and support is disproportionately small compared to its impact. It directs the Clerk of the House of Representatives to prepare copies of the resolution for distribution to the public and the press, so the recognition can be shared beyond the legislature.
What the bill does
- Formally recognizes February 28, 2026, as Turner Syndrome Awareness Day in Georgia.
- States legislative findings about Turner Syndrome, including its prevalence and associated health risks like aortic dissection and learning disabilities.
- Directs the Clerk of the House of Representatives to make copies of the resolution available to the public and the press.
- Does not create any new funding, program, or legal requirement; it is a symbolic statement rather than a change to Georgia law.
Who it affects
Women and girls diagnosed with or affected by Turner Syndrome, their families, medical specialists who treat the condition, and advocacy or research organizations focused on the disorder. The resolution also involves the Clerk of the House, who must distribute copies.
Why it matters
While the resolution creates no legal obligations or funding, it gives official state recognition to a condition the text says receives disproportionately little research funding, which can help raise public and medical awareness about early screening and health risks like aortic dissection.
Key provisions
- The whereas clauses describe Turner Syndrome as a non-inheritable chromosomal disorder linked to learning disabilities and a more than 100-fold increased risk of aortic dissection.
- The resolved clause formally designates February 28, 2026, as Turner Syndrome Awareness Day.
- A further resolved clause directs the Clerk of the House of Representatives to distribute copies of the resolution to the public and the press.
From the bill
“the associated risk for acute dissection, a life-threatening emergency caused by a tear in the aorta, is increased by more than 100-fold in young and middle-aged women with Turner Syndrome”
“despite the benefits of early screening, a disproportionately small amount of funding is available for Turner Syndrome research and support”
Status timeline
- House Read and Adopted (House)
- House First Readers (House)
- House Hopper (House)
Sponsors
- Charles Martin (R, HD-049)
Topics
- Turner Syndrome
- awareness day
- women's health
- genetic disorders
- rare disease