نتایج جستجو برای: maxillary deficiency

تعداد نتایج: 170106  

Journal: :iranian journal of medical sciences 0
chintamaneni raja lakshmi department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india sujana mulk bhavana department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india sai madhavi nallamilli department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india meka poorna venkata prabhat department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india gummadapu sarat department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india chennupati anuradha department of oral medicine and radiology,drs. sudha and nageswara rao siddhartha institute of dental sciences, gannavaram mandal, krishna district, andhra pradesh, india

ameloblastomas are slow growing, locally invasive, benign odontogenic tumors of an epithelial origin, accounting for approximately 1% of all oral tumors. a 40-year-old man presented with a chief complaint of a swelling over the left side of his face of 4 years’ duration. on examination, gross facial asymmetry was detected, and a well-defined swelling was noted intraorally involving the left max...

Journal: :Journal of clinical orthodontics : JCO 2003
Leon S Klempner

JCO/APRIL 2003 G patients with dentofacial deformities characterized by either a midfacial deficiency or true mandibular prognathism are perhaps the most challenging cases for the clinician to manage. In patients with midfacial deficiency, the current clinical protocol calls for orthopedic maxillary protraction by means of elastics to either an extraoral facemask or a chin cup.1,2 A maxillary e...

2016
Alessandro Ugolini Tiziana Doldo Luis T. Huanca Ghislanzoni Andrea Mapelli Roberto Giorgetti Chiarella Sforza

BACKGROUND The purpose of this controlled study was to investigate indirect effects on mandibular arch dimensions, 1 year after rapid palatal expansion (RPE) therapy. METHODS Thirty-three patients in mixed dentition (mean age 8.8 years) showing unilateral posterior crossbite and maxillary deficiency were treated with a RPE (Haas type) cemented on the first permanent molars. Treatment protocol...

Journal: :American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics 2002
Peter Ngan

During a 1981 presentation at an American Association of Orthodontists meeting, David Turpin recommended that early treatment should be considered for young patients who present with positive factors such as convergent facial type, anteroposterior functional shift, symmetrical condyle growth, mild skeletal disharmony, some remaining growth, good cooperation, no familial prognathism, and good fa...

Journal: :Plastic and reconstructive surgery 2015
Li Han Lai Brian K Hui Phuong D Nguyen Kristen S Yee Martin G Martz James P Bradley Justine C Lee

BACKGROUND Severe maxillary hypoplasia in cleft patients is caused by a combination of pathogenic and iatrogenic factors. In this work, the authors investigated anatomical deficiencies in dentition for predicting Le Fort I maxillary advancement surgery for severe maxillary hypoplasia in cleft patients. METHODS Cleft lip-cleft palate and cleft palate patients older than 14 years of age were re...

Journal: :APOS Trends in Orthodontics 2022

Objectives: Skeletally mature patients with transverse deficiency are best treated surgically assisted rapid palatal expansion (RPE) procedure. Recent studies have shown that microimplant-assisted RPE (MARPE) appliances can be effective in achieving skeletal young adults. This retrospective study aimed to evaluate the and dental alveolar changes response treatment MARPE three types of anteropos...

Journal: :Our Dermatology Online 2022

Apert syndrome is a rare which presents with craniosynostosis, severe syndactyly, and dysmorphic facial features. It mainly caused by new mutation in fibroblast growth factor receptor-2 gene. Up-regulation of this gene results bone fusion nuclear deficiency the transcription FoxO1 key pathogenesis acne. We present herein 19-year-old man nodulocystic acne associated acrocephaly, prominent forehe...

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