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Item Details
| Title:
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HEREDITARY RETINOPATHIES
PROGRESS IN DEVELOPMENT OF GENETIC AND MOLECULAR THERAPIES |
| By: |
Peter Humphries, Marian M. Humphries, Lawrence C.S. Tam |
| Format: |
Paperback |
| List price:
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£54.99 |
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We currently do not stock this item, please contact the publisher directly for
further information.
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| ISBN 10: |
1461444985 |
| ISBN 13: |
9781461444985 |
| Publisher: |
SPRINGER-VERLAG NEW YORK INC. |
| Pub. date: |
16 July, 2012 |
| Edition: |
2012 ed. |
| Series: |
Springerbriefs in Genetics 1 |
| Pages: |
46 |
| Description: |
The hereditary retinopathy, retinitis pigmentosa (RP), which affects 1 in 3,500 people worldwide, is the most common cause of registered visual handicap among those of the working age in developed countries. |
| Synopsis: |
The hereditary retinopathy, retinitis pigmentosa (RP), which affects 1 in 3,500 people worldwide, is the most common cause of registered visual handicap among those of the working age in developed countries. RP is a highly variable disorder where patients may develop symptomatic visual loss in early childhood, while others may remain asymptomatic until mid-adulthood. Most cases of RP segregate in autosomal dominant, recessive or X-linked recessive modes, with approximately 41 genes being implicated in disease pathology to date (RetNet). The extensive genetic heterogeneity associated with autosomal dominant RP (adRP) is an undisputed hindrance to the development of genetically based therapeutics. |
| Illustrations: |
3 black & white illustrations, 5 colour illustrations, biography |
| Publication: |
US |
| Imprint: |
Springer-Verlag New York Inc. |
| Returns: |
Returnable |
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