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Jun 11, 2024 · Pierre Robin Sequence is a congenital condition characterized by a series of developmental defects leading to upper airway obstruction and failure to thrive, either as part of a syndrome or in isolation.
5 days ago · Pierre Robin Syndrome (PRS) is one of the most common association in patients with OFC as already. identi ed in a previous study of our group 6. This syndrome is a congenital genetic abnormality.
Jun 29, 2024 · A receding chin may be a facial feature that runs in families or one associated with rare genetic disorders like Pierre-Robin Syndrome. The treatment may involve dental appliances, orthodontic headgear, and jaw or chin surgery.
4 days ago · The meaning of PIERRE ROBIN SYNDROME is a congenital defect of the face characterized by micrognathia, abnormal smallness of the tongue, cleft palate, and absence of the gag reflex and sometimes accompanied by bilateral eye defects, glaucoma, or retinal detachment.
4 days ago · Despite this prevalence, there is only one previously reported case that documents laryngomalacia and Pierre-Robin syndrome in a patient with Ohtahara syndrome . We present an additional case of upper airway abnormalities in a patient with Ohtahara syndrome.
Jun 17, 2024 · A systematic review of mandibular distraction osteogenesis versus orthodontic airway plate for airway obstruction treatment in Pierre Robin sequence. Cleft Palate Craniofac J. 2022;59(3):365-376. Crossref
5 days ago · Introduction: Pierre Robin sequence is characterized by the classic triad of congenital micrognathia, glossoptosis, and airway obstruction. It is caused by various etiologies, including cortical development malformations as seen in congenital perisylvian syndrome.
