Perioperative care of a patient with Beare-Stevenson syndrome

Paediatric Anaesthesia

Volumn 15, Issue 12, 2005, Pages 1131-1136

  Upmeyer, Sara ^a   Bothwell, Marcella ^a   Tobias, Joseph D ^a,b  

^a University of Missouri   (United States)

^b UNIVERSITY OF MISSOURI   (United States)

Author keywords

Anesthesia; Beare Stevenson; Choanal atresia; Craniosynostosis; Midface hypoplasia; Syndrome; Tracheal stenosis

Indexed keywords

BUPIVACAINE; CISATRACURIUM; FENTANYL; FIBROBLAST GROWTH FACTOR RECEPTOR 2; GLYCOPYRRONIUM BROMIDE; LIDOCAINE; PARACETAMOL; ROCURONIUM; SEVOFLURANE; THIOPENTAL;

ACANTHOSIS NIGRICANS; AMINO ACID SUBSTITUTION; ARTICLE; BEARE STEVENSON SYNDROME; CASE REPORT; CERVICAL SPINE; CHOANA ATRESIA; CLEFT PALATE; CRANIOFACIAL SYNOSTOSIS; EAR MALFORMATION; EXOPHTHALMOS; FACE DYSMORPHIA; FEMALE; FORAMEN MAGNUM; HUMAN; HYDROCEPHALUS; HYPERTELORISM; INFANT; PALPEBRAL FISSURE; PRIORITY JOURNAL; SKULL MALFORMATION; STRABISMUS; TRACHEA STENOSIS; ANESTHESIA; CRANIOFACIAL MALFORMATION; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; PERIOPERATIVE PERIOD; PRESCHOOL CHILD; SYNDROME;

ABNORMALITIES, MULTIPLE; ANESTHESIA; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; FEMALE; HUMANS; PERIOPERATIVE CARE; SYNDROME;

EID: 33644878682     PISSN: 11555645     EISSN: 14609592     Source Type: Journal    
DOI: 10.1111/j.1460-9592.2005.01585.x     Document Type: Article

References (18)

1. Beare JM, Dodge JA, Nevin NC. Cutis gyratum, acanthosis nigricans, and other congenital anomalies: a new syndrome. Br J Dermatol 1969 81: 241 247.
2. Stevenson RE, Ferlauto JG, Taylor HA. Cutis gyratum and acanthosis nigricans associated with other anomalies: a distinctive syndrome. J Pediatr 1978 92: 950 952.
3. Hall BD, Cadle RG, Golabi M et al. Beare-Stevenson cutis gyrata syndrome. Am J Med Genet 1992 44: 82 89.
4. Przylepa KA, Paxnekas W, Zhang M et al. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet 1996 13: 492 494.
5. Akai T, Iizuka H, Kishibe M et al. A case of Beare-Stevenson cutis gyrata syndrome confirmed by mutation analysis of the fibroblast growth factor receptor 2 gene. Pediatr Neurosurg 2002 37: 97 99.
6. Wang TJ, Huang CB, Tsai FJ et al. Mutation in the FGFR2 gene in a Taiwanese patient with Baere-Stevenson cutis gyrate syndrome. Clin Gen 2002 61: 218 221.
7. Roscioli T, Flanagan S, Mortimore RJ et al. Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3. Amer J Med Gen 2001 101: 187 194.
8. Lajeunie E, Catala M, Renier D. Craniosynostosis: from a clinical description to an understanding of bone formation of the skull. Childs Nervous System 1999 15: 676.
9. Butler MG. Hayes BG, Hathaway MM et al. Specific genetic diseases at risk for sedation/anesthesia complications. Anesth Analg 2000 91: 837 855.
10. Sleesman JB, Tobias JD. Anaesthetic implications of the child with Robinow syndrome. Paediatr Anaesth 2003 13: 629 632.
11. Tobias JD, Jones B, Jimenez DF et al. Anesthetic implications of Pfeiffer syndrome. Am J Anesth 1998 25: 79 83.
12. Vener DF, Lerman J. The pediatric airway and associated syndromes. Anesth Clin North Am 1995 13: 585 614.
13. Lauritzen C, Lilja J, Jarlstedt J. Airway obstruction and sleep apnea in children with craniofacial anomalies. Plast Reconstr Surg 1986 77: 1 5.
14. Kreiborg S, Barr M Jr., Cohen M. Jr. Cervical spine in the Apert syndrome. Am J Med Genet 1992 43: 704 708.
15. Berkowitz ID, Raja SN, Bender KS et al. Dwarfs: pathophysilogy and anesthetic implications. Anesthesiology 1990 73: 739 759.
16. Wang H, Rosenbaum ARE, Reid CS et al. Pediatric patients with achondroplasia: CT evaluation of the craniocervical junction. Radiology 1987 164: 515 519.
17. Wang TJ, Hung KS, Chen PKT et al. Beare-Stevenson cutis gyrata syndrome with Chiari malformation. Acta Neurochirurgica 2002 144: 743 745.
18. Ito S, Matsui K, Ohsak E et al. A cloverleaf skull syndrome probably of Beare-Stevenson type associated with Chiari malformation. Brain Dev 1996 18: 307 311.