Nooners Disease

Facial features include widely spaced eyes light colored eyes low set ears a short neck and a small lower jaw.

Nooners disease. It is characterized by mildly unusual facial features short stature heart defects bleeding problems skeletal malformations and many other signs and symptoms. 2020 word of the day inanition noun in uh nish uhn see definition. Noonan syndrome is a genetic disorder that prevents normal development in various parts of the body. Noonan syndrome is a rare genetic disorder.

A diagnosis of noonan syndrome is usually made after a doctor observes some key signs but this can be difficult because some features are subtle and hard to identify. Noonan syndrome is a genetic disorder that may cause short stature distinctive facial features and heart abnormalities. Description noonan syndrome is a condition that affects many areas of the body. The breast bone may either protrude or be.

Sometimes noonan syndrome isn t diagnosed until adulthood only after a person has a child who is more obviously affected by the condition. Turner like syndrome neonatology a group of specific abnormalities affecting both males and females both sporadic in appearance but also reflecting a hereditary component possibly ad clinical webbing of neck pectus excavatum facial defects low set or abnormally shaped ears ocular ptosis hypertelorism epicanthal folds micrognathia mild mental retardation short stature variable hearing loss delayed puberty undescended testicles small penis congenital heart. Heart problems may include pulmonary valve stenosis. A person can be affected by noonan syndrome in a wide variety of ways.

If you have it you might have certain identifiable facial features short height and unusual chest shape. Aside from face and heart abnormalities there may be associated bleeding abnormalities scoliosis infertility in males lymphedema and intellectual disability.