Retinal Dystrophy Gene Atlas / by Sarwar Zahid, Kari Branham, Dana Schlegel, Mark E. Pennesi, Michel Michaelides, John Heckenlively, Thiran Jayasundera
By: Zahid, Sarwar, autor
Contributor(s): Branham, Kari., autor. | Schlegel, Dana., autor. | Pennesi, Mark E., autor. | Michaelides, Michel., autor. | Heckenlively, John., autor. | Jayasundera, Thiran., autor.
Material type:
E-bookSeries: (Medicine (Springer-11650)).Publisher: Cham : Springer International Publishing, 2018Description: 1 recurso en línea (XIII, 279 páginas) : 169 ilustraciones, 163 ilustraciones a color.ISBN: 9783319108674.Subject: Degeneración macular | Retina -- EnfermedadesOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)
| Item type | Current library | Collection | Call number | Status | Date due | Barcode | Item holds | |
|---|---|---|---|---|---|---|---|---|
LIBRO-E NO PRÉSTAMO
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | RE661 .D3 2018 EB (Browse shelf(Opens below)) | Acceso electrónico | eBook.08112401 |
Part I. Autosomal Dominant Inheritance -- 1. BEST1 -- 2. CRX -- 3. CTRP5 -- 4. EFEMP1 -- 5. ELOVL4 -- 6. FSCN2 -- 7. GNAT1 -- 8. GUCA1A -- 9. GUCA1B -- 10. GUCY2D -- 11. IMPDH1 (RP10) -- 12. JAG1 -- 13. KLHL7 -- 14. PROM1 -- 15. PRPF3 (RP18) -- 16. PRPF31 -- 17. PRPF8 (RP18) -- 18. PRPH2 (RDS) -- 19. RBP3 -- 20. RGR -- 21. RHO -- 22. RLPB1 -- 23. RP1 -- 24. RIMS1 -- 25. SEMA4A -- 26. SNRNP200 -- 27. TIMP3 -- 28. TOPORS -- 29. TTC8 -- 30. VCAN -- 31. WFS1 -- Part II. Autosomal Recessive Inheritance -- 32. ABCA4 -- 33. AIPL1 -- 34. ALMS1 -- 35. ARL6 -- 36. BBS1 -- 37. BBS10 -- 38. BBS12 -- 39. BBS2 -- 40. BBS4 -- 41. BBS5 -- 42. BBS7 -- 43. BBS9 -- 44. C2ORF71 -- 45. C8ORF37 -- 46. CDH23 -- 47. CEP290 -- 48. CERKL -- 49. CLN3 -- 50. CLRN1 -- 51. CNGA1 -- 52. CNGA3 -- 53. CNGB1 -- 54. CNGB3 -- 55. CRB1 -- 56. CYP4V2 -- 57. DFNB31 -- 58. DHDDS -- 59. EYS -- 60. FAM161A -- 61. GNAT2 -- 62. GPR98 -- 63. IDH3B -- 64. IMPG1 -- 65. IQCB1 -- 66. KCNV2 -- 67. KCNJ13 -- 68. LCA5 -- 69. LRAT -- 70. MAK -- 71. MERTK -- 72. MYO7A -- 73. NMNAT1 -- 74. NR2E3 -- 75. NRL -- 76. OAT -- 77. PDE6A -- 78. PDE6B -- 79. PDE6C -- 80. PDE6G -- 81. PDE6H -- 82. PEX7 -- 83. PHYH -- 84. PRCD -- 85. RD3 -- 86. RDH5 -- 87. RDH12 -- 88. RPE65 -- 89. RPGRIP1 -- 90. SAG -- 91. SPATA7 -- 92. TULP1 -- 93. USH1C -- 94. USH1G -- 95. USH2A -- 96. ZNF513 -- Part III. X-Linked Inheritance -- 97. CACNA1F -- 98. CHM -- 99. NYX -- 100. OPN1LW -- 101. RP2 -- 102. RPGR -- 103. RS1.
Classically, photo atlases of retinal dystrophies have been divided into sections that describe and depict a particular retinal finding or disease, after which a differential diagnosis of potential diseases or mutated genes is provided. However, given the rapid improvement in molecular diagnostics, and the exponential increase in our understanding of the phenotypes caused by each mutated gene, the paradigm has changed. Physicians are now more interested in the variable expressivity associated with mutations in each individual gene. Therefore, Retinal Dystrophy Gene Atlas catalogs the different phenotypes that have been reported with each mutated gene. Each section describes a gene and its known clinical phenotypes and features of disease, along with retinal photos of affected patients. Written by prominent retinal dystrophy specialists from the largest dystrophy centers worldwide, Retinal Dystrophy Gene Atlas contains more than 80 chapters, each of which describes the clinical and photographic manifestations of a specific gene. The chapters include stunning clinical color photographs of the retina, autofluorescence imaging, electrophysiologic findings, and cross-sectional imaging. Retinal Dystrophy Gene Atlas serves as a resource to aid genetic diagnosis in patients with retinal dystrophies.
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