Page 43 - Clinical variability in Noonan syndrome with emphasison ear and eye
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                OCULAR MANIFESTATIONS OF NOONAN SYNDROME: A PROSPECTIVE STUDY OF 25 PATIENTS
Conclusion
NS is a clinical diagnosis with multiple genetic bases, associated with an extensive variety of congenital ocular abnormalities. Ocular features of NS are characterized by one or more developmental anomalies of the eyelids (involving the position, opening and closure), associated with various other ocular abnormalities in childhood, including amblyopia, myopia, astigmatism, strabismus, limited ocular motility, prominent corneal nerves, and posterior embryotoxon.
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