Noonan Syndrome Diagnosis & Treatment Market Growth and Sales Forecast 2018–2026
Noonan syndrome is a rare genetic disorder. Scientists believe that Noonan syndrome can cause a wide range of other physical and developmental symptoms that usually start at birth. They say that four genes are involved in Noonan syndrome, PTPN11, RAF1, SOS1, and KRAS. Common symptoms associated with Noonan syndrome are widely spaced eyes, extra skin on the neck, small lower jaw, low-set nipples, excessive bruising, delayed puberty, vision or hearing problems, puffy feet and hands (in infants), thickening of heart...
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