Noonan Syndrome Research

www.genome.gov/25521674
www.noonansyndrome.org
www.mayoclinic.com/health/noonan-syndrome/DS00857
www.betterhealth.vic.gov.au/bhcarticles.nsf/pages/Noonan_syndrome
www.norditropinhcp.com
www.specialchild.com
www.mayoclinic.com










10.) there is no cure but it is highly recommended to keep up on medicines and treatments








 9.) noonan syndrome support group



















8.) there are many treatments such as heart, vision, and lymphatic treatments

7.) other symptoms such as growth issues, musculoskeletal issues, learning disabilities, eye problems, bleeding, lymphatic problems, and geneital and kidney probelems












6.) symptoms: skin problems and curly or sparse hair












5.) symptoms: heart defects













4. sympotoms: facial features a key clinical feature that leads to diagonsis










3.) changes in one of several autosomal dominant genes, ex: there are 7 genes known of that can cause noonan syndrome, 4 are the PTPN11, SOS1, RAF1,and the KRAS genes, there are several more to be discovered









2.) what is noonan syndrome? it is a disorder that involves unusual facial features, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformation of the bones of the rib cage

1.) title page: The Noonan Syndrome

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