Apert Syndrome
Apert Syndrome
Comprehensive Care of the Patient and Family
Alonso, Nivaldo; Meara, John G.; Proctor, Mark R.
Springer Nature Switzerland AG
04/2026
672
Dura
Inglês
9783032125507
Pré-lançamento - envio 15 a 20 dias após a sua edição
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Section I. General Principles.- Introduction.- Eugene Apert: More than a Simple Syndrome.- Head and Neck and Extremity Anatomy.- Molecular Genetics and Pathophysiology.- Clinical Genetic Aspects.- Diagnosis and Imaging.- Section II. Surgical Management.- Perioperative and Anesthesia Management.- Ophthalmic Evaluation.- Surgery on the Eyes and Eyelids.- Otologic Disorders.- Cleft Palate.- Orthodontic Care.- Airway Assessment and Management.- Neurosurgical Considerations.- Early Surgery: Endoscopic Strip Craniectomy (ESC).- Management of the Posterior Vault.- Two-Stage Strategy: FOA and Le Fort III.- Monobloc Advancement with Internal Distraction.- Monobloc Advancement with External Distraction.- Midface Management: The CHOP Approach and the Role of Monobloc with Le Fort II Advancement.- Hypertelorism Correction: Monobloc Facial Bipartition with Internal Distraction.- Hypertelorism Correction: Box Osteotomy.- Segmental Subcranial Midface Osteotomies: Le Fort II with Zygomatic Repositioning.- Le Fort III Distraction with or without Facial Bipartition.- Orthognathic Surgery I.- Orthognathic Surgery II.- Virtual Surgical Planning for Orthognathic Surgery.- Aesthetic Refinements.- Aesthetic Refinements During Adolescence.- Innovations and Emerging Technologies in Craniofacial Surgery.- Surgical Treatment of the Apert Hand.- Management of the Apert Foot.- Section III. Patient, Family, and Community.- Neurocognitive Implications, Etiological Mechanisms, and Clinical Care Recommendations.- Social and Psychological Impacts and Recommendations.- Living with Apert Syndrome: Patient Perspectives.- Caring for a Child with Apert Syndrome: Family Perspectives, Advocacy, and Support.- Economic Considerations for the Treatment of Syndromic Craniosynostosis.- Global Health Policy and Advocacy.
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Apert syndrome;cranial surgery;craniofacial surgery;maxillofacial surgery;syndactyly surgery;genetic disorder;craniofacial abnormality;hydrocephalus;monobloc;hypertelorism;Open Access
Section I. General Principles.- Introduction.- Eugene Apert: More than a Simple Syndrome.- Head and Neck and Extremity Anatomy.- Molecular Genetics and Pathophysiology.- Clinical Genetic Aspects.- Diagnosis and Imaging.- Section II. Surgical Management.- Perioperative and Anesthesia Management.- Ophthalmic Evaluation.- Surgery on the Eyes and Eyelids.- Otologic Disorders.- Cleft Palate.- Orthodontic Care.- Airway Assessment and Management.- Neurosurgical Considerations.- Early Surgery: Endoscopic Strip Craniectomy (ESC).- Management of the Posterior Vault.- Two-Stage Strategy: FOA and Le Fort III.- Monobloc Advancement with Internal Distraction.- Monobloc Advancement with External Distraction.- Midface Management: The CHOP Approach and the Role of Monobloc with Le Fort II Advancement.- Hypertelorism Correction: Monobloc Facial Bipartition with Internal Distraction.- Hypertelorism Correction: Box Osteotomy.- Segmental Subcranial Midface Osteotomies: Le Fort II with Zygomatic Repositioning.- Le Fort III Distraction with or without Facial Bipartition.- Orthognathic Surgery I.- Orthognathic Surgery II.- Virtual Surgical Planning for Orthognathic Surgery.- Aesthetic Refinements.- Aesthetic Refinements During Adolescence.- Innovations and Emerging Technologies in Craniofacial Surgery.- Surgical Treatment of the Apert Hand.- Management of the Apert Foot.- Section III. Patient, Family, and Community.- Neurocognitive Implications, Etiological Mechanisms, and Clinical Care Recommendations.- Social and Psychological Impacts and Recommendations.- Living with Apert Syndrome: Patient Perspectives.- Caring for a Child with Apert Syndrome: Family Perspectives, Advocacy, and Support.- Economic Considerations for the Treatment of Syndromic Craniosynostosis.- Global Health Policy and Advocacy.
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