|
| | HR0460 | | LRB103 34972 MST 64864 r |
|
|
1 | | HOUSE RESOLUTION |
2 | | WHEREAS, Turner Syndrome is a rare and non-inheritable |
3 | | chromosomal condition that occurs when the secondary X |
4 | | chromosome is partially or completely missing for those born |
5 | | female; and |
6 | | WHEREAS, More than 98% of fetuses with Turner Syndrome |
7 | | will die before birth, resulting in about 10% percent of all |
8 | | first trimester miscarriages; and |
9 | | WHEREAS, Turner Syndrome affects approximately one in |
10 | | 2,000 female live births worldwide; and |
11 | | WHEREAS, Three in 10 individuals diagnosed with Turner |
12 | | Syndrome have Mosaic Turner Syndrome, for which the number of |
13 | | X chromosomes can vary; and |
14 | | WHEREAS, There are over 85,000 people living with Turner |
15 | | Syndrome in the United States, and more than 30% of |
16 | | individuals born with Turner Syndrome are not diagnosed until |
17 | | they are 15 years old, with only 3.5% receiving adequate care; |
18 | | and |
19 | | WHEREAS, Those living with Turner Syndrome often face |
20 | | lifelong cognitive, emotional, physical, and psychological |