Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. (17/46)

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Polysomnography evaluation and swallowing endoscopy of patients with Pierre Robin sequence. (18/46)

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Syndromes of the first and second branchial arches, part 2: syndromes. (19/46)

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Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate. (20/46)

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Airway management in neonates with Pierre Robin sequence. (21/46)

Neonates with Pierre Robin sequence (PRs) suffer from varying degrees of airway obstruction and feeding difficulties, the courses of which differ from patient to patient, due to mandibular deficiency. We aimed to evaluate the course and prognosis of upper airway obstruction in 20 newborns with PRs. Among 15 isolated and 5 syndromic cases, 7 patients fell into Group I, 5 into Group II and 8 into Group III, respectively, according to the clinical classification system proposed by Caouette-Laberge. The 12 patients in Groups I and II were treated with positioning and gavage feeding, whereas the 6 patients in Group III underwent bilateral mandibular distraction. Decannulation or avoidance of tracheostomy was achieved in all of them. A patient who had a significant comorbidity was managed with tracheostomy and one patient expired due to pulmonary problems. When conservative measures fail, mandibular distraction osteogenesis should be considered to obviate tracheostomy in newborns with micrognathia.  (+info)

Abnormal fetal movements, micrognathia and pulmonary hypoplasia: a case report. Abnormal fetal movements. (22/46)

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Physiologic and clinical benefits of noninvasive ventilation in infants with Pierre Robin sequence. (23/46)

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Pierre Robin sequence: report of two cases. (24/46)

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