The Noonan syndrome by Stephanie Lopez Hernandez https://padlet.com/s80288/4i4lqdki1mss This is a gene-based en-us 2019-03-12 20:58:46 UTC 2026-01-10 17:43:12 UTC hello@padlet.com Causes of Noonan syndrome s80288 https://padlet.com/s80288/4i4lqdki1mss/wish/340639897 ¨Mutations in multiple genes can cause Noonan syndrome.¨

The main point
-Gene mutation cause Noonan Syndrome

mutations cause an additional 10 to 15 percent.]]> 2019-03-12 21:26:56 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/340639897 Kid having the Noonan syndrome s80288 https://padlet.com/s80288/4i4lqdki1mss/wish/344990559 Click the blank to get to the link (story)👇👇👍]]> 2019-03-25 19:21:29 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/344990559 DESCRIPTION s81200 https://padlet.com/s80288/4i4lqdki1mss/wish/360075328 Noonan syndrome affects many areas in the body, facial features, short stature, heart defects, bleeding problems, skeletal malfunctions and other signs. Many people with noonan syndrome have easy and noticable facial features. 50% of people with noonan syndrome have short stature. Most people are also born with a heart defect wich also causes a lot of bleeding. some people with noonan syndrome could get learning disablilities later in life. Other people may get diagnosed with cancer. Noonan syndrome is in a group called RASopathies many other sickneses in this group have similar symptoms]]> 2019-05-14 19:21:04 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/360075328 NOONAN SYNDROME s81200 https://padlet.com/s80288/4i4lqdki1mss/wish/360076357 TYPE: GENE
GENE: PTPN11PROTEIN AFFECTED:the protiens encoded by these genes are members of the RAS-MAPK signaling pathway]]> 2019-05-14 19:23:44 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/360076357 Frequency and Inheritance pattern s99077 https://padlet.com/s80288/4i4lqdki1mss/wish/360077445 Frequency- Noonan syndrome occurs in approximately 1 in 1,000 to 2,500 people.

Inherhertance pattern - This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.]]> 2019-05-14 19:26:20 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/360077445 s81200 https://padlet.com/s80288/4i4lqdki1mss/wish/360510738 2019-05-15 18:58:08 UTC https://padlet.com/s80288/4i4lqdki1mss/wish/360510738