This video is about a rare genetic disorder Noonan Syndrome. I have discussed the etiology and clinical manifestations. Most common symptoms of Noonan syndrome include short stature, webbing of neck, pectus carinatum or pectus excavatum, cubitus valgus, pulmonary stenosis, wide set eyes, epicanthal folds, down-slanting palpebral fissures, ptosis, micrognathia, and ear abnormalities. There may be clinodactyly, hepatosplenomegaly and high-frequency sensorineural hearing loss. Males frequently have cryptorchidism. Adult height is usually achieved at end of the second decade and it reaches almost at lower limit of normal.
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