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    Allogenous cartilage graft versus autogenous cartilage graft in augmentation rhinoplasty: A decade of clinical experience
    (SPRINGER, 2008) Tosun, Z.; Karabekmez, F. E.; Keskin, M.; Duymaz, A.; Savaci, N.
    Cartilage grafts have great value in augmentation rhinoplasty. For most surgeons, an autogenous cartilage graft is the first choice in rhinoplasty because of its resistance to infection and resorption. On the other hand, an allogenous cartilage graft might be preferred over an autogenous graft to avoid additional morbidity and lengthened operating time. Allogenous cartilage grafts not only have the advantage of averting donor site morbidity but also are resistant to infection, resembling autogenous cartilage grafts. The authors present their experience with 41 patients who underwent augmentation rhinoplasty using 22 autogenous and 19 allogenous cartilage grafts between June 1994 and August 2004. For evaluation of adequate augmentation rates, photographic analyses were performed on preoperative, early postoperative, and late postoperative photographs from all the patients. To assess patient satisfaction, the Facial Appearance Sorting Test (FAST) was applied preoperatively and late postoperatively in both groups. These results were compared, and it was concluded that in terms of resorption, there was no difference in the early and late postoperative follow-up data between allogenous and autogenous cartilage grafts. Evaluation of the preoperative and early postoperative photographic outcomes showed statistically significant differences with respect to adequate augmentation rates between the two groups. The FAST scores showed statistically significant differences between preoperative and late postoperative outcomes. There were no infections in the two groups of patients.
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    A Case of a New Syndrome or a Variant of the Rare Popliteal Pterygium Syndrome
    (2001) Öğün, T. C.; Tosun, Z.; Arazi, M.; Kapıcıoğlu, Safa
    The popliteal pterygium syndrome is very rare, and is characterized by a congenital popliteal web accompanying the genitourinary, craniofacial, and musculoskeletal anomalies. We described a case of presumably popliteal pterygium syndrome with severe right popliteal web, right renal agenesis, left bifurcated ninth rib, urethral orifice in the vagina, right presacral discoloration resembling A-V malformation, imperforate anus, skin dimple in the left gluteal region, right calcaneovalgus foot with supernumerary digits and aberrant profunda femoris artery. This is the first report of this combination in the pertinent literature.
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    Murray-Puretic Syndrome: A Report of Two Cases
    (SPRINGER VERLAG, 1998) Savacı, N.; Gökalp, A.; Yenidünya, M. O.; Tosun, Z.
    The Murray-Puretic Syndrome is also known as juvenile hyaline fibromatosis. It is a congenital disorder characterized by skin lesions, joint contractures, gingival hypertrophy and bone lesions. Two siblings with this syndrome are presented.