Laryngotracheal anomalies in children with craniofacial syndromes

Journal of Craniofacial Surgery

Volumn 13, Issue 2, 2002, Pages 351-363

  Papay, Frank A ^a   McCarthy, Vincent P ^a   Eliachar, Isaac ^a   Arnold, James ^b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRONCHOMALACIA; CHILD; CLEFT LARYNX; COMORBIDITY; CRANIOFACIAL MALFORMATION; HUMAN; LARYNGOMALACIA; LARYNX ATRESIA; LARYNX DISORDER; LARYNX HYPOPLASIA; LARYNX MALFORMATION; LARYNX STENOSIS; LARYNX WEB; PRIORITY JOURNAL; RESPIRATORY TRACT MALFORMATION; REVIEW; TRACHEA DISEASE; TRACHEA MALFORMATION; TRACHEA STENOSIS; TRACHEOMALACIA; VOCAL CORD PARALYSIS;

EID: 0036336495     PISSN: 10492275     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001665-200203000-00036     Document Type: Review

References (67)

1. Obstructive sleep apnea patients have craniomandibular abnormalities
2. Airway obstruction and sleep apnea in children with craniofacial anomalies
3. The management of otolaryngological problems in the mucopolysaccharidoses: A retrospective review
4. Apert's syndrome and palatal mucopolysaccharides
5. Mutations in fibroblast growth factor receptors: Phenotypic consequences during eukaryotic development
6. The pathology of some malformations and hereditary diseases of the respiratory tract
7. Genetics of craniofacial malformation
8. Obstructive sleep apnea in Apert's and Pfeiffer's syndromes: More than a craniofacial abnormality
9. Multiple congenital anomalies associated with a 47XXX chromosome constitution
10. Hypomandibular faciocranial dysostosis: Report of an affected sib and follow-up
11. Tracheal agenesis: Recognition and management
12. Otolaryngologic features of malformation syndrome with cryptophthalmos
13. Partial unilateral cryptophthalmos with syndactyly, brachycephaly and renal anomalies
14. Marshall-Smith syndrome: Two case reports and a review of pulmonary symptoms
15. Congenital malformations associated with maternal use of valporic acid
16. Toriello-Carey syndrome: Report of a new case
17. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: A new autosomal recessive syndrome?
18. Brief clinical report: Anomalies in an infant with Nager acrofacial dysostosis
19. Dysmorphic facies, omphalocele, laryngeal and pharyngeal hypoplasia, spinal anomalies, and learning disabilities in a new dominant malformation syndrome
20. Neonatal stridor with Larsen's syndrome
21. Larsen's syndrome: A skeletal dysplasia with multiple joint dislocations and unusual facies
22. A patient with Larsen syndrome
23. Larsen's syndrome
24. Laryngomalacia and intra-neural striated muscle in an infant with the Freeman-Sheldon syndrome
25. Evaluation of epiglottoplasty as treatment for severe laryngomalacia
26. Otolaryngological manifestations of arthrogryposis multiplex congenita
27. The anaesthetic management of an infant with frontometaphyseal dysplasia (Gorlin-Cohen syndrome)
28. Klippel-Feil syndrome associated with malformed larynx
29. The larynx in the Cri du Chat syndrome
30. Anaesthetic considerations in Down's syndrome: Experience with 100 patients and a review of the literature
31. Ventilatory management assisted by cardiopulmonary bypass for distal tracheal resuscitation in a neonate
32. Fraser syndrome: A case report and review of the otolaryngologic manifestations
33. ENT abnormalities associated with Fraser syndrome: Case report and literature review
34. ENT manifestations of Fraser syndrome
35. Fronto-metaphyseal dysplasia. Further delineation of the clinical syndrome
36. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: Velo-cardial-facial syndrome
37. The G syndrome/Opitz oculo-genital-laryngeal syndrome/Opitz BBB/G syndrome/Opitz-Frias syndrome
38. Congenital hypothalamic hamarblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly- A new syndrome? Part 1. Clinical, causal, and pathogenetic considerations
39. Anomalies of the tracheal cartilage. Report of 6 cases and review of the literature
40. Symmetrical bronchial pattern with normal atrial morphology
41. Case conference: Case 1-1991
42. Association of Down syndrome and segmental tracheal stenosis with ring tracheal cartilages: A review of nine cases
43. Tracheobronchial anomalies in children
44. Fryn's syndrome in a girl born to consanguineous parents. A case report
45. Anatomical abnormalities in mandibulofacial dysostosis
46. Rib-gap defect with micrognathia, malformed tracheal cartilages, and redundant skin: A new pattern of defective development
47. de la Chapelle dysplasia
48. Synchrondrosen des laryngotrachrealskeletts and tracheostenose beim Apert-Crouzon syndrome
49. Cloverleaf skull syndrome. An autopsy case and review of literatures
50. The cloverleaf skull anomaly: Managing extreme cranio-orbito-facio stenosis
51. Tracheal stenosis in Apert's syndrome
52. Completely cartilaginous trachea in a child with Crouzon syndrome
53. Vertically fused tracheal cartilage: An underrecognized anomaly
54. Congenital tracheal stenosis in Pfeiffer syndrome
55. Tracheal cartilaginous sleeve
56. Upper and lower airway compromise in the Apert syndrome
57. An infant with Crouzon's syndrome with a cartilaginous trachea and a human tail
58. A lethal Larsen-like multiple joint dislocation syndrome
59. Atelostenogenesis Type 3: The first patient in Japan and a survivor for more than 1 year
60. Tracheomalacia in Hallermann-Streiff syndrome
61. Verification of the fetal valproate syndrome phenotype
62. Fryn's syndrome: Brief clinical report
63. Metatropic dwarfism, the Kniest syndrome and the pseudochondroplastic dysplasias
64. Cryptorchidism, chest deformities, and other congenital anomalies in three brothers
65. Chondroectodermal dysplasia (Ellis van Creveld syndrome) with bronchial malformation and neonatal tension lobar emphysema
66. Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia
67. Tracheomalacia and bronchomalacia associated with Larsen syndrome