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BONE DYSPLASIAS‚ An atlas of genetic disorders of skeletal development

BONE DYSPLASIAS- An atlas of genetic disorders of skeletal development-9780195396089
  1. Autor:

    Spranger

  2. Isbn:

    9780195396089

  3. Páginas:

    1456

  4. Año:

    2012

  5. Edición:

    3

  6. Idioma:

    Ingles

  7. Disponibilidad:

    Agotado

Precio s/iva:

209.88 €

199,39  €
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DESCRIPTION:
Since the publication of the second edition on Bone Dysplasias ten years ago, there has been an explosion of knowledge about skeletal dysplasias. The molecular basis of a great number of disorders has been delineated, and many new conditions have been recognized. Now more than ever, the importance of accurate diagnosis cannot be overstated. Given the growth of activity and research in the field, practitioners must acknowledge that many conditions with superficial similarities have different inheritance patterns and prognoses. Various research and routine laboratories can pinpoint specific diagnoses, but before the appropriate laboratory can be consulted and eventual costs considered, clinical and radiographic features must be identified with a high degree of precision.

Fully updated and expanded, this new edition of Bone Dysplasias contains:

- More than 100 chapters on newer entities to assist the practitioner in narrowing a group of diagnostic possibilities to a specific disorder
- Over 2,500 diagnostic radiographs with concise clinical and biological information on a total of 275 rare constitutional skeletal diseases
- Concise data on the etiopathogenesis, natural course, complications, and differential diagnosis of rare conditions

A true landmark in the study and investigation of bone dysplasias, this comprehensive volume will be a must-have resource radiologists, medical geneticists, orthopedic surgeons, pediatricians, and genetic counselors caring for patients with bone dysplasias.

CONTENTS:
Section I Skeletal Dysplasias with Predominant Metaphyseal Involvement
1. FGFR3 Group
2. Metaphyseal Dysplasia Schmid type
3. Cartilage-hair-Hypoplasia
4. Metaphyseal Dysplasia Spahr type
5. Shwachman-Diamond Syndrome
6. Omenn Syndrome
7. Metaphyseal Anadysplasia
8. Metaphyseal Acroscyphodysplasia
9. Jansen Dysplasia
10. Eiken Dysplasia
11. CINCA

Section II Skeletal Dysplasias with Predominant Epiphyseal Involvement
12. Sulfate Transporter Group
13. Multiple Epiphyseal Dysplasia, autosomal dominant
14. Pseudoachondroplasia

Section III Chondrodysplasia Punctata Group
15. Greenberg Dysplasia
16. Chondrodysplasia punctata, X-linked dominant
17. Congenital hemidysplasia, ichthyosis, limb deficiency (CHILD)
18. Chondrodysplasia punctata, autosomal recessive
19. Chondrodysplasia punctata, X-linked recessive
20. Chondrodysplasia punctate, autosomal dominant type
21. Chondrodysplasia punctata, tibial-metacarpal type

Section IV Skeletal Dysplasias with Prominent Diaphyseal Involvement
22. Filamin A Group
23. Filamin B Group

Section V Spondylo-Epiphyseal Dysplasias
24. Type 2 Collagen Group
25. Type 11 Collagen Group
26. Perlecan Group
27. Spondyloepiphyseal Dysplasia tarda, X-linked
28. Spondyloepiphyseal Dysplasia tarda, autosomal recessive
29. Spondyloepiphyseal Dysplasia, Kimberley type
30. Spondyloepiphyseal Dysplasia, Wolcott-Rallison type
31. Immunoosseous Dysplasia
32. Progressive Pseudorheumatoid Chondrodysplasia
33. Spondylo-Megaepiphyseal-Metaphyseal Dysplasia

Section VI Spondylo-Metaphyseal Dysplasias
34. Spondylometaphyseal Dysplasia, Sedaghatian type
35. Odontochondrodysplasia
36. Spondylometaphyseal Dysplasia, Sutcliffe (corner fracture) type
37. Spondyloenchondrodysplasia
38. Spondylometaphyseal Dysplasia with cone-rod dystrophy
39. Axial Spondylometaphyseal Dysplasia

Section VII Spondylo-Epi-Metaphyseal Dysplasias
40. TRPV4 Group
41. Brachyolmia, autosomal recessive
42. Dyggve-Melchior-Clausen Dysplasia
43. Spondylo-epi-metaphyseal Dysplasia, short limb abnormal calcification type
44. SPONASTRIME Dysplasia
45. Spondylo-epi-metaphyseal Dysplasia, leptodactylic type
46. Chondrodysplasia with congenital joint dislocations, CST3 type
47. Desbuquois Dysplasia
48. gPAPP Dysplasia
49. Pseudodiastrophic Dysplasia
50. Spondylo-epi-metaphyseal Dysplasia with joint laxity

Section VIII Severe Spondylodysplastic Dysplasias
51. Achondrogenesis type 1A
52. Schneckenbecken Dysplasia
53. Opsismodysplasia

Section IX Short-rib (-Polydactyly) Dysplasias
54. Asphyxiating Thoracic Dysplasia
55. Chondroectodermal Dysplasia
56. Thoracopelvic Dysplasia (Barnes)
57. SRP, Saldino-Noonan-Verma-Naumoff type
58. SRP, Beemer-Langer type
59. SRP, Majewski type
60. Orofaciodigital syndrome IV Mohr-Majewski

Section X Rhizomelic/Mesomelic Dysplasias
61. Omodysplasia
62. Robinow Syndrome
63. Dyschondrosteosis
64. Langer Mesomelic Dysplasia
65. Mesomelic Dysplasia, Kantaputra type
66. Werner Mesomelic Dysplasia
67. Mesomelic Dysplasia, Kozlowski-Reardon type
68. Mesomelic Dysplasia, Nievergelt-Savarirayan type
69. Mesomelic Dysplasia with acral synostoses

Section XI Acromesomelic Dysplasias
70. Acromesomelic Dysplasia, Maroteaux type
71. Grebe Dysplasia

Section XII Acromelic Dysplasias
72. Isolated Brachydactylies
73. Trichorhinophalangeal Dysplasia I
74. Trichorhinophalangeal Dysplasia II
75. Acrocapitofemoral Dysplasia
76. Angel-shaped phalangoepiphyseal Dysplasia
77. Albright Osteodystrophy
78. Acrodysostosis
79. Marshall-Smith Syndrome
80. Geleophysic Dysplasia
81. Acromicric Dysplasia
82. Cranioectodermal Dysplasia (Sensenbrenner)
83. Saldino-Mainzer Dysplasia
84. Familial digital arthropathy with brachydactyly

Section XIII Bent Bone Dysplasias
85. Campomelic Dysplasia
86. Cousin Dysplasia
87. Cumming Dysplasia

Section XIV Slender Bone Dysplasias
88. Three-M Syndrome
89. Kenny-Caffey Dysplasia
90. Microcephalic Osteodysplastic Primordial Dwarfism, type 1
91. Microcephalic Osteodysplastic Primordial Dwarfism, type 2
92. IMAGE Syndrome
93. Osteocraniosteosis

Section XV Dense Bone Dysplasias with Normal Bone Shape
94. Blomstrand Dysplasia
95. Osteopetroses
96. Dysosteosclerosis
97. Pyknodysostosis
98. Osteomesopyknosis
99. Osteopetrosis, Ectodermal Dysplasia, Immune Defect OLEDAID
100. Osteopoikilosis
101. Melorheostosis
102. Osteopathia striata with cranial sclerosis

Section XVI Dense Bone Dysplasias with Meta-Diaphyseal Modeling Defects
103. Caffey Infantile Hyperostosis
104. Osteoectasia with hyperphosphatasia
105. Endosteal Hyperostosis, van Buchem type
106. Diaphyseal dysplasia, Camurati Engelmann
107. Diaphyseal Dysplasia with Anemia (Ghosal)
108. Lenz-Majewski Hyperostotic Dysplasia
109. Pachydermoperiostosis
110. Hypertrophic Osteoarthropathy Currarino
111. Diaphyseal Medullar Stenosis with Bone Malignancy
112. Sclerosteo-cerebellar Syndrome
113. Craniodiaphyseal Dysplasia
114. Craniometaphyseal Dysplasia
115. Pyle disease
116. Metaphyseal Dysplasia, Braun-Tinschert type
117. Oculodentoosseous Dysplasia
118. Trichodentoosseous Dysplasia

Section XVII Dysplasias with Decreased Bone Density
119. Osteogenesis imperfecta
120. Juvenile Idiopathic Osteoporosis
121. Bruck Syndrome
122. Singleton-Merten Syndrome
123. Geroderma osteodysplasticum
124. Weismann-Netter Toxopachyosteosis
125. Calvarial doughnut lesions with bone fragility
126. Cole-Carpenter Dysplasia
127. Spondylo-ocular Dysplasia
128. Gnathodiaphyseal dysplasia

Section XVIII Dysplasias with Defective Mineralization
129. Hypophosphatasia
130. Neonatal Hyperparathyroidism
131. Hereditary Rickets

Section XIX Lysosomal Storage Diseases with Skeletal Involvement(Dysostosis multiplex)
132. Mucopolysaccharidoses
133. Muclipidoses
134. Oligosaccharidoses

Section XX Osteolyses
135. Familial Expansile Osteolysis
136. Infantile Systemic Hyalinosis/Juvenile Fibromatosis
137. Mandibuloacral Dysplasia
138. Progeria Huchinson-Gilford
139. Winchester-Torg Syndrome
140. Hajdu-Cheney Syndrome
141. Multicentric Carpo-Tarsal Osteolysis

Section XXI. Disorganized Development of Skeletal Components
142 Fibrous Dysplasia
143. Cherubism
144. Progressive Osseous Heteroplasia
145. Multiple Cartilaginous Exostoses
146. Osteoglophonic Dysplasia
147. Fibrodysplasia Ossificans Progressiva
148. Dysplasia Epiphysealis Hemimelica
149. Enchondromatosis (Ollier)
150. Cheirospondyloenchondromatosis
151. Genochondromatosis
152. Metachondromatosis

Section XXII Cleidocranial Dysplasias
153. Cleidocranial Dysplasia
154. Yunis-Varon Syndrome
155. CDAGS Syndrome

Section XXIII Craniosynostosis Syndromes (selected)
156. Apert Syndrome
157. Pfeiffer Syndrome
158. Antley-Bixler Syndrome
159. Saethre-Chotzen Syndrome
160. Baller-Gerold Syndrome
161. Carpenter Syndrome
162. Muenke Syndrome

Section XXIV Costovertebral Dysostoses (selected)
163. Spondylocostal Dysostoses
164. Jarcho-Levin Syndrome
165. Cerebro-costo-mandibular Syndrome
166. Ischio-spinal Dysostosis

Section XXV Limb A/Hypoplasias (seleced)
167. Roberts Syndrome
168. Ectrodactyly-Ectodermal Dysplasias
169. Femoral Hypoplasia-Unusual Facies Syndrome
170. Femur-Fibula-Ulna Syndrome
171. Nail-Patella Syndrome
172. Ischio-Patellar Dysplasia

Section XXVI Acral and other Dysostoses (selected)
173. Keutel Syndrome
174. Catel-Manzke Syndrome
175. Poland Syndrome
176. Greig Cephalopolysyndactyly Syndrome

Section XXVII Disorders caused by Defective Joint Formation
178. Multiple Synostosis Syndrome



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