![]() ![]() Other eye problems are also common, including increased pressure within the eye ( glaucoma ), clouding of the lens of the eyes ( cataracts ), and tearing of the lining of the eye ( retinal detachment ). In some cases, the clear gel that fills the eyeball (the vitreous ) has an abnormal appearance, which is noticeable during an eye examination. Many people with Stickler syndrome have severe nearsightedness (high myopia ), which means they have trouble seeing things that are far away. This combination of features can lead to feeding problems and difficulty breathing. Pierre Robin sequence includes an opening in the roof of the mouth (a cleft palate ), a tongue that is placed further back than normal (glossoptosis), and a small lower jaw ( micrognathia ). A particular group of physical features called Pierre Robin sequence is also common in people with Stickler syndrome. This appearance results from underdeveloped bones in the middle of the face, including the cheekbones and the bridge of the nose. These signs and symptoms vary widely among affected individuals.Ī characteristic feature of Stickler syndrome is a somewhat flattened facial appearance. doi: 10.1016/j.ijporl.2005.07.Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems. Prognosis of airway obstruction and feeding difficulty in the Robin sequence. The effectiveness of mandibular distraction in improving airway obstruction in the pediatric population. Tahiri Y, Viezel-Mathieu A, Aldekhayel S, Lee J, Gilardino M. Surgical airway management in Pierre Robin sequence: is there a role for tongue-lip adhesion? Cleft Palate Craniofac J. ![]() The surgical correction of Pierre Robin sequence: mandibular distraction osteogenesis versus tongue-lip adhesion. Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Mechanisms of airway obstruction in Robin sequence: implications for treatment. The aetiology and pathogenesis of craniofacial deformity. Etiopathogenesis of isolated Robin sequence. Incidence of the Robin Anomalad (Pierre Robin syndrome). A fall of the base of the tongue considered as a new cause of nasopharyngeal respiratory impairment: Pierre Robin sequence, a translation. International Journal of Oral and Maxillofacial Surgery. Precise osteotomies for mandibular distraction in infants with Robin sequence using virtual surgical planning. Tip: Most babies outgrow these difficulties by 6 months due to mandibular growth and improved control of the tongue. The mortality associated with these symptoms is between 1.7 and 11.3% 11. This is performed to rule out other anatomical sites or causes of airway obstruction Prior to any surgical intervention, a nasoendoscopy is recommended.
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