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Oral manifestations of inherited disorders /
Oral Manifestations of Inherited Disorders.
| Clasificación: | Libro Electrónico |
|---|---|
| Autores principales: | , , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Boston :
Butterworths,
�1977.
|
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Cover image; Title page; Table of Contents; Copyright; Preface; Chapter 1: Genetic Counseling and Oral Examination; Publisher Summary; 1.1 Genetic Counseling; 1.2 Physical Examination of the Oral Cavity; 1.3 Radiologic Interpretation of Some Oral and Paraoral Structures; Chapter 2: Some Inherited Conditions Affecting Only Calcified Dental Tissue; Publisher Summary; 2.1 Amelogenesis Imperfecta; 2.2 Coronal Dentin Dysplasia; 2.3 Hereditary Opalescent Dentin; 2.4 Radicular Dentin Dysplasia; Chapter 3: Systemic Inherited Disorders with Dental Involvement; Publisher Summary; 3.1 Acroosteolysis
- 3.2 Amelocerebrohypohidrosis Syndrome3.3 Cryptodontic Brachymetacarpalia; 3.4 Hypodontia and Nail Dysgenesis; 3.5 Hypophosphatasia (Phosphoethanolaminuria); 3.6 Hypophosphatemic Vitamin D-Resistant Rickets; 3.7 Hypoplastic-Hypocalcified Enamel, Onycholysis, and Functional Hypohidrosis; 3.8 Incontinentia Pigmenti; 3.9 Oculodentoosseous Dysplasia; 3.10 Otodental Syndrome; 3.11 Pseudohypoparathyroidism and Pseudopseudohypoparathyroidism; 3.12 Rothmund-Thomson Syndrome; Chapter 4: Systemic Inherited Disorders with Oral or Perioral Soft Tissue Involvement; Publisher Summary
- 4.1 Acrodermatitis Enteropathica4.2 Bloom Syndrome; 4.3 Ch�ediak-Higashi Syndrome; 4.4 Congenital Indifference to Pain; 4.5 Cutis Laxa; 4.6 Cyclic Neutropenia; 4.7 Double Lip, Blepharochalasis, and Nontoxic Thyroid Enlargement; 4.8 Dyskeratosis Congenita with Pigmentation, Dystrophic Nails, Aplastic Anemia, and Leukoplakia Oris; 4.9 Fabry Syndrome; 4.10 Familial Dysautonomia; 4.11 Gingival Fibromatosis with Ear, Nose, Bone, and Nail Defects and Hepatosplenomegaly; 4.12 Gingival Fibromatosis with Hypertrichosis, Epilepsy, and Mental Retardation
- 4.13 Gingival Fibromatosis with Multiple Hyaline Fibromas4.14 Hereditary Benign Intraepithelial Dyskeratosis; 4.15 Hereditary Hemorrhagic Telangiectasia; 4.16 Hermansky-Pudlak Syndrome; 4.17 Hyperkeratosis Palmoplantaris and Attached Gingival Hyperkeratosis; 4.18 Lesch-Nyhan Syndrome; 4.19 Moebius Syndrome; 4.20 Multiple Hamartoma and Neoplasia Syndrome; 4.21 Multiple Mucosal Neuromas, Medullary Carcinoma of the Thyroid, Pheochromocytoma, and Marfanoid Body Build with Muscle Wasting; 4.22 Neurofibromatosis; 4.23 Pachydermoperiostosis; 4.24 Pachyonychia Congenita, Jadassohn-Lewandowski Type
- 4.25 Peutz-Jeghers Syndrome4.26 Pseudoxanthoma Elasticum; 4.27 Xerodermic Idiocy; 4.28 White Sponge Nevus; Chapter 5: Systemic Inherited Disorders with Involvement of Jaw Bones; Publisher Summary; 5.1 Apert Syndrome; 5.2 Carpenter Syndrome; 5.3 Cerebrohepatorenal Syndrome; 5.4 Cherubism; 5.5 Chondrodysplasia Punctata; 5.6 Craniofacial Dysostosis; 5.7 Craniometaphyseal Dysplasia and Craniodiaphyseal Dysplasia; 5.8 Infantile Cortical Hyperostosis; 5.9 Mandibulofacial Dysostosis; 5.10 Marfan Syndrome; 5.11 Melnick-Needles Syndrome; 5.12 Mucopolysaccharidosis VII; 5.13 Pfeiffer Syndrome