Results 91 to 100 of about 12,301 (210)
Temporomandibular joint (TMJ) ankylosis is a joint disorder characterized by the fibrotic or bony adhesion of anatomical joint components, leading to severe limitation or loss of joint mobility.
TAKAMURA, Yutaro +5 more
core +1 more source
Objective: To investigate the feasibility and reproducibility of the prenasal thickness (PNT)/nasal bone length (NBL) ratio, maxilla-nasion-mandible (MNM) angle, facial profile line, profile line distance, and prefrontal space ratio (PFSR) in the first ...
Bakker, Merel +5 more
core +1 more source
Dental management of Goldenhar syndrome in a pediatric patient
The purpose of the case report was to highlight the various features of Goldenhar syndrome to aid in the diagnosis of this syndrome which has classic clinical features such as microtia, preauricular skin tags, micrognathia, facial asymmetry, midface ...
Asmita Das +4 more
doaj +1 more source
Pierre Robin Sequence (PRS) is a rare congenital condition characterized by micrognathia, glossoptosis, and often cleft palate, predisposing patients to severe airway management difficulties.
Min Joo Shin, Jin Huh
doaj +1 more source
Ankylosis of the temporomandibular joint in children is one the most difficult and complex conditions managed by oral and maxillofacial surgeons, and often leads to some facial deformity.
Pereira Filho, Valfrido Antonio +3 more
core +1 more source
Pierre Robin and the Treatment of Micrognathia – Glossoptosis
Level of evidence: 5 – expert ...
Andrew C. Li +2 more
openaire +2 more sources
- There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma.
Hosein Shabni Mirzaee +5 more
core
https://scholarlyexchange.childrensmercy.org/care_models/1041/thumbnail ...
Children\u27s Mercy Kansas City
core
Hypoglossia-hypodactylia (Hanhart's) syndrome with sensorineural hearing loss
Hanhart's syndrome, an uncommon disorder characterized by severe micrognathia, hypoglossia and absence of the extremities, belongs to the oromandibular-limb hypogenesis group of diseases. Our patient was admitted with the complaints of abnormality
B Tüysüz +3 more
doaj
Extreme Airway Difficulty During EXIT in Severe Fetal Agnathia: Failed Conventional Intubation and Successful Emergency Tracheostomy-A Case Report. [PDF]
Muawad R +7 more
europepmc +1 more source

