000 02288nam a22002895i 4500
001 402877
003 ES-MaUEC
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008 231212s2023 sz | o |||| 0|eng d
020 _a9783031409264
024 7 _a10.1007/978-3-031-40926-4
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aRK529-535
_b2023 EB
245 0 0 _aFacial Reconstruction of Unusual Facial Clefts :
_bA Guide to Diagnosis and Treatment
_cedited by Nivaldo Alonso, Renato da Silva Freitas, Cristiano Tonello, Philippe Pellerin
250 _a1st ed. 2023
264 1 _aCham
_bSpringer International Publishing
_c2023
300 _a1 recurso en línea
336 _atexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
505 0 _a1. Introduction -- 2. Genetics in Unusual Facial Clefts -- 3. Mechanisms, aetiology and classification of rare clefts -- 4. Cleft 0-14 -- 5. Cleft 1-13 -- 6. Cleft 2-12 -- 7. Cleft 3-11 -- 8. Cleft 4 -- 9. Cleft 5 -- 10. Cleft 6 -- 11. Cleft 7 -- 12. Cleft 8 -- 13. Cleft 9 -- 14. Cleft 10 -- 15. Cleft 30.
520 _aFacial cleft is one of the most common congenital anomalies while atypical facial clefts are rare, with an incidence of 1.43 and 4.85 in 100,000 births. This book is dedicated exclusively to the diagnosis and treatment of rare facial clefts. It provides a comprehensive review of clinical aspects and surgical approaches used in unusual facial clefts and associated syndromes. Moreover, presents different classifications and surgical techniques, reflecting the authors extensive experience with a broad cross-section of treated patients. The rich illustrations and computed tomography images allows a broad view, helping the reader to understand the conduct in complex cases. Facial Reconstruction of Unusual Facial Clefts is an indispensable reference for all healthcare professionals involved in the multidisciplinary treatment of patients with craniofacial anomalies.
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-031-40926-4
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
988 _aSpringer_Medicine_2023
999 _c402877
_d402877