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J Craniofac Surg
October 2024
Division of Plastic and Oral Surgery, Baylor Scott and White Medical Center and McLane Children's Hospital, Temple, TX.
Noonan syndrome (NS) is a rare, genetic multisystem disorder often presenting with associated craniofacial abnormalities. The authors report an identical twin pair with classical features of NS including short stature, mild ptosis, hypertelorism, down-slanting palpebral fissures, low-set angulated ears, and giant cell tumors in the craniofacial skeleton. Interestingly, these patients also presented with bilateral, symmetric, dystrophic auricular calcifications.
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