Craniofacial Structures in Connective Tissue Disorders
Seiten
1990
John Wiley & Sons Inc (Verlag)
978-0-471-56688-5 (ISBN)
John Wiley & Sons Inc (Verlag)
978-0-471-56688-5 (ISBN)
- Titel ist leider vergriffen;
keine Neuauflage - Artikel merken
Offers a detailed study of the developmental aspects of craniofacial dysmorphology and covers various clinical and basic aspects of the craniofacial structure in connective tissue disorders. Topics include mast cells in bone remodelling and molecular basis among hereditary dentinal defects.
This volume offers a detailed study of the developmental aspects of craniofacial dysmorphology, covering various clinical and basic aspects of the craniofacial structure in connective tissue disorders. Specific topics covered include: molecular basis among hereditary dentinal defects; prospective management of cervicomedullary compression in achondroplasia; mast cells in bone remodeling; terminology of craniofacial anomalies. Detailed discussions also offer clinically-relevant information on the craniofacial manifestations of such syndromes as Ehlers-Danlos, Cutis Laxa, Cutis Luxa-like and Marfan.
This volume offers a detailed study of the developmental aspects of craniofacial dysmorphology, covering various clinical and basic aspects of the craniofacial structure in connective tissue disorders. Specific topics covered include: molecular basis among hereditary dentinal defects; prospective management of cervicomedullary compression in achondroplasia; mast cells in bone remodeling; terminology of craniofacial anomalies. Detailed discussions also offer clinically-relevant information on the craniofacial manifestations of such syndromes as Ehlers-Danlos, Cutis Laxa, Cutis Luxa-like and Marfan.
In Honor of David Bixler (M. Melnick); Acknowledgment and Comments (D. Bixler); Molecular Basis Among Hereditary Dentinal Defects: Pathobiology of Dentinal Phosphophoryn (J. Sauk); Mast Cells in Bone Remodeling: Using a Genetically Defined Mouse Model as a Clue to Human Disease (R. Rosenstein, et al.); Terminology of Craniofacial Anomalies (J. Opitz); Craniofacial Manifestations of Ehlers-Danlos Syndromes, Cutis Laxa Syndromes, and Cutis Laxa-Like Syndromes (R. Gorlin & M. Cohen); Craniofacial Aspects of the Marfan Syndrome (A. Poole); The Prospective Management of Cervicomedullary Compression in Achondroplasia (I. Thomas & J. Frias); Index.
Reihe/Serie | Birth Defects: Original Article S. ; Vol 25, no 4 |
---|---|
Zusatzinfo | Ill. |
Verlagsort | New York |
Sprache | englisch |
Maße | 35 x 55 mm |
Gewicht | 369 g |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete |
Studium ► 2. Studienabschnitt (Klinik) ► Pathologie | |
ISBN-10 | 0-471-56688-8 / 0471566888 |
ISBN-13 | 978-0-471-56688-5 / 9780471566885 |
Zustand | Neuware |
Haben Sie eine Frage zum Produkt? |
Mehr entdecken
aus dem Bereich
aus dem Bereich