New York J 258: Memorializing Governor Kathy Hochul to proclaim February 2025, as Turner Syndrome Awareness Month in the State of New York

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J00258 Summary:

BILL NOJ00258 

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SAME ASNo Same As

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SPONSORPALUMBO

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COSPNSR

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MLTSPNSR

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Go to top J00258 Actions:

BILL NOJ00258 

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01/22/2025REFERRED TO FINANCE

01/28/2025REPORTED TO CALENDAR FOR CONSIDERATION

01/28/2025ADOPTED

Go to topJ00258 Committee&nbspVotes:

Go to topJ00258 Floor&nbspVotes:

There are no Assembly votes for this bill in this legislative session.

Go to topJ00258 Text:

Assembly Resolution No. 91

BY: M. of A. Schiavoni

 MEMORIALIZING Governor Kathy Hochul to proclaim
 February 2025, as Turner Syndrome Awareness Month in
 the State of New York

 WHEREAS, It is the custom of this Legislative Body to recognize
official months that are set aside to increase awareness of serious
health issues that affect the lives of citizens of New York State; and

 WHEREAS, Attendant to such concern, and fully in accord with its
long-standing traditions, this Legislative Body is justly proud to
memorialize Governor Kathy Hochul to proclaim February 2025, as Turner
Syndrome Awareness Month in the State of New York, in conjunction with
National Turner Syndrome Awareness Month; and

 WHEREAS, Turner Syndrome is the second most common genetic disorder,
affecting 1 in 2,000 females; over 1,000 baby girls are born with the
Syndrome annually; and

 WHEREAS, Discovered in 1938 by Dr. Henry Turner, Turner Syndrome is
a genetic condition that can only affect people born female; instead of
the usual 46 chromosomes a person is born with, those with Turner
Syndrome have cells that are missing all or part of an X chromosome; and

 WHEREAS, In about half of all individuals with Turner Syndrome, the
affected female has only one X chromosome; others may have two X
chromosomes, but one is incomplete; sometimes a female has some cells
with two X chromosomes, but other cells have only one; and

 WHEREAS, Most fetuses (98-99%) with Turner Syndrome will die before
birth, and the genetic disorder is contributed to about 10% of all
first-trimester miscarriages; and

 WHEREAS, More than 30% of individuals with Turner Syndrome are not
diagnosed until they are 15 years old, and only 3.5% receive adequate
care; with increased awareness, the lives of those affected can be
drastically improved; and

 WHEREAS, In 2025, there are over 85,337 individuals living with
Turner Syndrome in the United States; it is estimated that an
approximate 5,028 women in New York State have the genetic disorder; and

 WHEREAS, Ultimately, the specific cause of Turner Syndrome is
unknown because the gene on the X chromosome that is responsible for
most of the features of the chromosomal disorder is undetermined;
however, researchers have been able to identify the gene responsible for
short stature and skeletal abnormalities, which is the SHOX gene,
important for bone development and growth; and

 WHEREAS, The signs of Turner Syndrome should be detected during a
girl's first few years of life for the best possible outcomes for
treatment; a variety of signs allude to the possibility of an individual
having this condition, such as a short stature and frequent ear

infections, which should signal the need for diagnostic testing for the
disorder; and

 WHEREAS, There are many health concerns associated with a diagnosis
of Turner Syndrome, including: potentially fatal cardiovascular
diseases; reduced cognitive function; educational issues consisting of
difficulty with visual spatial tasks, memory, attention, as well as
other learning disabilities; risk of ovarian failure; type II diabetes;
hyporthyroidism; psychological issues like low self-esteem,
predisposition to age-specific problems, isolation, depression;
pregnancy complications; and hearing issues, along with many other
complications; and

 WHEREAS, Symptoms that are prevalent among females with Turner
Syndrome often go untreated because of lack of education about the
signs, symptoms and possible treatments to improve overall quality of
life outcomes; by spreading awareness about this condition, those
affected by Turner Syndrome may be treated earlier to produce long-term
positive outcomes for the patient; and

 WHEREAS, Founded in 2008, the Turner Syndrome Foundation supports
research initiatives and facilitates educational programs that increase
professional awareness a