(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
Progerin causes the nuclear envelope to become unstable and disrupt nuclear shape
Severe arteriosclerosis (hardening of arteries) begins in childhood
The mutation leads to production of an abnormal protein called progerin
Children appear normal at birth but show signs of aging within the first two years and live up until their teen years.
Increased risk of heart attack and stroke at a young age
Development of farnesyltransferase inhibitors (FTIs) to block progerin’s harmful effects have shown promise in clinical trials by improving some symptoms
Affects about 1 in 4 million newborns worldwide
Medicines can help protect the heart and improve quality of life
Emerging gene editing approaches like CRISPR hold future potential
First described in the late 19th century, named after Hutchinson and Gilford
LMNA gene produces lamin A, a protein essential for maintaining the structure of the cell nucleus
Clinical trials show improved cardiovascular health and lifespan extension
Cells age faster and die prematurely, especially in connective tissues and blood vessels which explains skin aging, joint problems, and cardiovascular disease
A rare genetic disorder causing rapid aging in children
Progerin disrupts the cell’s nucleus, causing premature cell aging
Hair loss (alopecia) and aged-looking skin
Growth failure: children grow slower and weigh less than peers
This leads to DNA damage and impaired cell division
Intellectual development and motor skills remain normal
Caused by a mutation in the LMNA gene on chromosome 1
Characteristic facial appearance: prominent eyes, thin nose with beaked tip, small chin, protruding ears
There is no cure yet, but doctors can help with symptoms
Discovery of the LMNA mutation in 2003 was a major milestone
Research continues to focus on slowing disease progression and improving life quality
Doctors also suggest healthy food and exercise for children with progeria
Cellular aging accelerated, mimicking aspects of normal aging at molecular level
Major cause of death in progeria patients, usually in their teens