Results 91 to 100 of about 112,270 (166)

Facio-genito-popliteal syndrome presenting with bilateral choanal atresia and maxillary hypoplasia

open access: yes, 2000
The most classic characteristics of facio-genito-popliteal syndrome are cleft lip and/or palate, anomalies of the external genitalia and popliteal pterygium.
Urbain, Frédéric   +5 more
core   +1 more source

Spontaneous Mandibular Dentoalveolar Changes after Rapid Maxillary Expansion (RME), Slow Maxillary Expansion (SME), and Leaf Expander—A Systematic Review

open access: yesChildren
Background: This systematic review aims to analyze the spontaneous dentoalveolar changes in the mandibular arch after maxillary expansion in growing patients obtained with different expansion protocols: Rapid Maxillary Expansion (RME), Slow Maxillary ...
Alessandro Ugolini   +6 more
doaj   +1 more source

B2-Mandibular Retrognathism and Maxillary Alveolar Protrusion (Class II, Division 1/2)

open access: yes
Sagittal mandibular retrognathism (mandibular deficiency/hypoplasia/retrognathia) as basic deviation may occur in combination with various maxillary deformities: + Sagittal maxillary excess (maxillary prognathism/midface hyperplasia) Vertical maxillary ...
Lie, Suen An Nynke   +2 more
core   +1 more source

Rapid maxillary expansion effects on masticatory muscle activity: A systematic review and meta-analysis

open access: yesJournal of Orthodontic Science
This systematic review aims to assess the impact of rapid maxillary expansion (RME) on masticatory muscle activity through electromyographic analysis. A systematic review was conducted according to the Cochrane Collaboration guide.
Gabriela Leite Pedroso   +10 more
doaj   +1 more source

Bilateral maxillary sinus hypoplasia

open access: yesMajmaah Journal of Health Sciences
Maxillary sinus hypoplasia is an uncommon condition characterized by underdevelopment of the maxillary sinus antrum. Typically, it is accompanied by other anomalies, such as abnormalities in the uncinate process and infundibular passage. We present a rare case of bilateral maxillary sinus hypoplasia in a 22-year-old, symptomatic patient who didn’t ...
openaire   +1 more source

A Rare Complication Associated with Distraction Osteogenesis in Correction of Maxillary Hypoplasia

open access: yes, 2017
Aim: Distraction osteogenesis (DO) is an alternative to orthognathic surgery that appears to have some advantages for advancement in the maxilla and mandible, but relatively high complication rates have been reported in the maxillofacial region. ...
Serdar Yenigün   +2 more
core   +1 more source

Incidental Detection of Maxillary Sinus Hypoplasia on Cone-beam Computed Tomography: a Case Report

open access: yes
Maxillary sinus hypoplasia is defined as the underdevelopment of the maxillary sinus, resulting in a smaller-than-normal sinus volume. It may remain asymptomatic and be detected incidentally during radiographic examinations or may occasionally present ...
Menduh KAYA
core   +1 more source

Facemask therapy with rigid anchorage in a patient with maxillary hypoplasia and severe oligodontia

open access: yes, 2003
In this report, we describe the treatment of a 10-year-old girl with a Class III skeletal relationship with maxillary hypoplasia and severe oligodontia. The maxillary arch was in a complete crossbite relationship with the mandibular arch.
Iplikcioglu, H   +3 more
core   +1 more source

A2-Mandibular Prognathism and Vertical Maxillary Excess-VME (Mostly Class III)

open access: yes
Sagittal mandibular prognathism (mandibular excess) as basic deviation may occur in combination with various maxillary deformities: + Sagittal maxillary deficiency (maxillary retrognathism/midface hypoplasia) Vertical maxillary excess Vertical maxillary ...
Lie, Suen An Nynke   +2 more
core   +1 more source

Clinical case seminar - Hypogonadotropic hypogonadism as a presenting feature of late-onset X-linked adrenal hypoplasia congenita [PDF]

open access: yes, 2002
Mutations in the orphan nuclear receptor DAX-1 cause X-linked adrenal hypoplasia congenita. Affected boys usually present with primary adrenal failure in early infancy or childhood.
Beck-Peccoz, P   +8 more
core  

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