The role of genioplasty in the management of craniofacial deformities

نویسندگان

  • Shaheel Chummun
  • PJ Anderson
چکیده

The function of a genioplasty is to produce an aesthetically pleasing chin contour and improve facial proportions. The aim of this study was to review the role of osseous genioplasty in the management of patients with craniofacial deformities. 52 patients (24 males and 28 females) treated at the Australian Craniofacial Unit in Adelaide, Australia over a 25-year period; who required a genioplasty as part of their craniofacial management were reviewed. Patients ranged from 17-44 years (median: 26 years) and the age at which the patients underwent genioplasty was between 9 and 36 years (median: 17 years). Pre and 6 months post op cephalograms were compared, showing a mean chin advancement of 7mm and a mean osseous resorption of 20%. One patient was under-corrected and another had post-operative asymmetry, both requiring repeat genioplasty. No long-term nerve dysfunction was noted. The osseous genioplasty is an effective procedure for correcting the chin deformity often seen in patients with craniofacial abnormalities. It is an easy technique to master and is associated with a low degree of morbidity.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Assessing Patient-Reported Outcomes Following Orthognathic Surgery and Osseous Genioplasty.

Primary outcomes for orthognathic surgery and genioplasty patients include satisfaction with appearance, improved motor function, and enhanced quality of life. The goal of this study was to assess outcomes among patients undergoing these procedures, and to highlight the potential use of FACE-Q instrument for use in patients with dentofacial deformities. A total of 56 patients presenting for ort...

متن کامل

Orthognathic Surgery in Craniofacial Microsomia: Treatment Algorithm

Craniofacial microsomia is a broad term that covers a variety of craniofacial malformation conditions that are caused by alterations in the derivatives of the first and second pharyngeal arches. In general terms, diverse therapeutic alternatives are proposed according to the growth stage and the severity of the alteration. When craniofacial growth has concluded, conventional orthognathic surger...

متن کامل

کرانیوفاسیال دیسوستوزیس و گزارش یک مورد جراحی سندرم کروزون

The most important craniofacial dysostosis & syndromes are Crouzon, Apret, Pfeiffer.Carpenter Saether- Chotzen. The common characteristic is premature closure of cranial sutures, which result in Maxillofacial deformities. Perfect recognition and carefully evaluation are the most important points in their reconstruction surgery.Because the prevalence & surgical treatment of Crouzon syndrome is l...

متن کامل

Ectopic Ciliated Cyst in the Mandible Secondary to Genioplasty and Lefort after Two Years: A Case Report and Literature Review

Introduction: The ectopic ciliated cyst is a rare non-odontogenic cyst which occurs as a delayed complication after maxillary sinus radical surgery; this lesion emerges due to the destruction of the sinus mucosa during the surgery and entrapment of the respiratoryepitheliumin the region. This lesion has been observed in very rare cases following genioplasty and bimaxillary orthognathic surgery....

متن کامل

The Art of Genioplasty: An Insight

Approximately 20% of the population is affected by dentofacial deformities which may demonstrate myriad degrees of functional and aesthetic compromise. Moderate to severe occlusal discrepancies most often require combined orthodontic treatment and orthognathic surgery to attain the most stable results with optimal function and aesthetic outcomes. Orthognathic surgery is said to be the art and s...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013