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Journal of the Korean Cleft Palate-Craniofacial Association ; : 136-138, 2005.
Article Dans Coréen | WPRIM | ID: wpr-220666

Résumé

Ullrich-Noonan syndrome was first recognized as a unique entity in 1963 when Noonan and Ehmke described a series of patients with unusual faces and multiple malformations. These patients proved to have phenotypes of Turner syndrome with normal karyotyes, which is important feature that distinguishes Noonan from Turner syndrome. Typical features are triangular shaped face, hypertelorism, down slanting eyes, ptosis, strabismus, amblyopia, refractive errors, low set ears with thickened helices, high nasal bridge and webbed neck. A 5-year old female was admitted to our center for a surgical intervention of the known webbed neck deformity, ipsilateral upper eyelid ptosis and bilateral epicanthal fold. She had normal karyotye(46, XX) without further abnormality on physical examination. We corrected the webbed neck deformity, ptosis and epicanthal fold simultaneously with satisfactory result.


Sujets)
Enfant d'âge préscolaire , Femelle , Humains , Amblyopie , Blépharoptose , Malformations , Oreille , Hypertélorisme , Cou , Syndrome de Noonan , Phénotype , Examen physique , Ptérygion , Troubles de la réfraction oculaire , Strabisme , Syndrome de Turner
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