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Noonan syndrome - Symptoms and causes - Mayo Clinic Noonan syndrome is a genetic condition that stops typical development in various parts of the body It can affect a person in several ways, including unusual facial features, short height, heart problems and other physical problems
Noonan Syndrome - StatPearls - NCBI Bookshelf Noonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations Gene mutations involve the RAAS MAPK (mitogen-activated protein kinase) signaling pathway The patient presentation can range from mild to severe
Noonan Syndrome (Leopard Syndrome): Causes Outlook - Cleveland Clinic Noonan syndrome is a genetic condition that can affect many parts of your child’s body While symptoms vary widely, they most often include unusual facial features, short stature and heart problems Early detection and treatment can ease symptoms and prevent complications What is Noonan syndrome?
About Noonan Syndrome - National Human Genome Research Institute Noonan syndrome is a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformations of the bones of the rib cage What is Noonan Syndrome?
Noonan syndrome - MedlinePlus Noonan syndrome is a condition that affects many areas of the body It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms
Noonan syndrome | Craniofacial Anomalies | UC Davis Childrens Hospital Noonan syndrome is an autosomal dominant condition This means that if you have the condition there is a 1 in 2 or 50% chance with each pregnancy that you will pass it on to your child This is a very variable syndrome
Noonan Syndrome - Boston Childrens Hospital Noonan syndrome is a genetic condition that can affect many different areas of the body and development Children who have Noonan syndrome often have recognizable facial features and physical characteristics such as short stature
Noonan Syndrome - Childrens Health Issues - The Merck Manuals Noonan syndrome is caused by mutations in certain genes that can be inherited from a parent who has an affected gene It also can occur spontaneously in a child whose parents do not have an affected gene