Heart problems are treated in the same way as they are for individuals in the general population. Children with Niemann-Pick disease type A generally do not survive past early childhood.
Top of page What is the treatment for Noonan syndrome? In addition, the common symptoms of lung cancer can differ between smokers and non-smokers, with a vague sensation of shortness of breath often attributed to aging or inactivity being a common symptom among those who have not smoked.
Genetics Home Reference. What are your concerns? Finding Reliable Health Information Online A listing of information and links for finding comprehensive genetics health information online. The affected children develop normally until around age 1 year when they experience a progressive loss of mental abilities and movement psychomotor regression.
High incidence of Noonan syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p. Because these lipids are not in their proper location in cells, many normal cell functions that require lipids such as cell membrane formation are impaired. These features may be more pronounced in infants and young children, but change with age.
If this fits you, talk to your doctor about screening.
Orphanet J Rare Dis. Unfortunately, whether people are celebrities or not, the stigma of the disease has prevented many people from talking openly about their diagnosis.
Genotype-phenotype correlation. Acid sphingomyelinase is responsible for the conversion of a fat lipid called sphingomyelin into another type of lipid called ceramide. It's hoped that going forward, more celebrities with lung cancer will come forward, without the fear of the stigma of the disease. Some forms of congenital heart disease associated with this disorder include:.
Back to Health A-Z. This content does not have an Arabic version. Treatment for individuals who have Noonan syndrome is based on their particular symptoms.