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TGFBI-related Corneal Dystrophies -

TGFBI-related Corneal Dystrophies

Clinical Findings, Cell Biology, and Genetics
Buch | Hardcover
128 Seiten
2025 | 2025 ed.
Springer Nature Switzerland AG (Verlag)
9789819601301 (ISBN)
CHF 149,75 inkl. MwSt
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This book provides up-to-date information about the basic cell biology, protein processing mechanisms, genetics, and treatment strategies for TGFBI-related corneal dystrophies. Descriptions of metabolic pathways involving TGFBI protein include recent information about the intracellular processing of normal and mutated TGFBI proteins.

This book provides up-to-date information about the basic cell biology, protein processing mechanisms, genetics, and treatment strategies for TGFBI-related corneal dystrophies.  Extensive illustrations document the clinical appearance of these dystrophies, and details of their cell biology provide our current understanding of intracellular pathologic mechanisms related to the mutated TGFBI protein.  Descriptions of metabolic pathways involving TGFBI protein include recent information about the intracellular processing of normal and mutated TGFBI proteins.  Detailed descriptions of the pathologic basis for TGFBI-related corneal dystrophies and possible strategies for human gene therapy are provided.  This book offers a rich source of information about the pathogenesis, diagnosis, and treatment options for practicing ophthalmologists, specialists, and trainees.

Eung Kweon Kim, MD, PhD, Emeritus, Department of Ophthalmology, Severance Hospital, Seoul, KoreaR. Doyle Stulting, MD, PhD, Director, Stulting Research Center, Emeritus, Department of Ophthalmology, Emory University, USA

1. Introduction.- 2. What is TGFBIp and what is its function?.- a.What are TGFBI corneal dystrophies.-I. History of TGFBI corneal dystrophies in Europe.- 3. Classification and mutations of TGFBI Corneal Dystrophies.- a. Dystrophies with deposits primarily in Bowman layer.- I. Reis-Bücklers corneal dystrophy (RBCD).- II. Thiel-Behnke corneal dystrophy (TBCD).- b. Dystrophies with deposits primarily in the stroma.- I. Lattice corneal dystrophy with TGFBI mutation.- II. Classic lattice corneal dystrophy (Lattice corneal dystrophy type 1; LCD1).- III. Variants of lattice corneal dystrophy (III, IIIA, I/IIIA, and IV).- c. Granular corneal dystrophy.- I. Granular corneal dystrophy type 1 (GCD1).- II. Granular corneal dystrophy type 2 (GCD2, Avellino CD, Combined granular lattice CD).- 4. Molecular pathogenesis of GCD2 and TGFBI corneal dystrophies.- 5. Proteolysis of TGFBIp.- 6. Genetics and gene therapy on the TGFBI corneal dystrophies.

Erscheinungsdatum
Zusatzinfo 58 Illustrations, color; 7 Illustrations, black and white
Verlagsort Cham
Sprache englisch
Maße 178 x 254 mm
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Augenheilkunde
Naturwissenschaften Biologie Genetik / Molekularbiologie
Schlagworte Gene therapy of corneal dystrophy • Molecular biology of corneal dystrophy • Pathogenesis of corneal dystrophy • TGFBI and refractive surgery • Treatment of corneal dystrophy
ISBN-13 9789819601301 / 9789819601301
Zustand Neuware
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