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Retinal dystrophy gene atlas

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Retinal dystrophy gene atlas/ by Sarwar Zahid ... [et al.].
其他作者:	Zahid, Sarwar.
出版者:	Cham :Springer International Publishing : : 2018.,
面頁冊數:	xiii, 279 p. :digital ; : 24 cm.;
Contained By:	Springer eBooks
標題:	Retinal degeneration - Atlases. - Genetic aspects -
電子資源:	http://dx.doi.org/10.1007/978-3-319-10867-4
ISBN:	9783319108674

Retinal dystrophy gene atlas
Retinal dystrophy gene atlas[electronic resource] /by Sarwar Zahid ... [et al.]. - Cham :Springer International Publishing :2018. - xiii, 279 p. :digital ;24 cm.

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.

ISBN: 9783319108674

Standard No.: 10.1007/978-3-319-10867-4doiSubjects--Topical Terms:

1206573
Retinal degeneration
--Genetic aspects--Atlases.

LC Class. No.: RE661.D3

Dewey Class. No.: 617.735

Retinal dystrophy gene atlas
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505 0 $a 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.
520 $a 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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