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A comprehensive review on Ichthyosis

a family of genetic skin disorders
Buch | Softcover
140 Seiten
2019
AV Akademikerverlag
978-620-2-00431-2 (ISBN)
CHF 86,65 inkl. MwSt
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The Ichthyosis are a large, clinically, genetically, and etiologically heterogeneous group of disorders of cornification due to abnormal differentiation and desquamation of the epidermis. Although they differ in clinical features, inheritance, and structural and biochemical abnormalities of the epidermis, they often pose a diagnostic challenge. These skin disorders are the result of the presence of excessive amounts of dry surface scales due to marked keratinization or cornification, as a consequence of abnormal epidermal differentiation and metabolism. To date, five major types of IT have been officially described, which include ichthyosis vulgaris, lamellar ichthyosis, epidermolytic hyperkeratosis, congenital ichthyosiform erythroderma, and X-linked ichthyosis. These can be differentiated based on the general clinical manifestations, histological findings, as well as genetic makeup. The molecular findings reveal the functional importance and interactions of many different epidermal proteins and metabolic pathways, including major structural proteins (keratins, loricrin), enzymes involved in lipid metabolism, peroxisomal transport and processing and DNA repair.

Nahid, Sumaiya
I am Sumaiya Nahid, lecturer, department of Pharmacy, University of Science and Technology Chattagram,Bangladesh. My research interests are structure based drug design, bio-assay guided isolation and pharmacological screening of plants.

Erscheinungsdatum
Sprache englisch
Maße 150 x 220 mm
Themenwelt Medizin / Pharmazie Pharmazie
Schlagworte Case history • Ichthyosis • Mechanism • pathophysiology
ISBN-10 620-2-00431-2 / 6202004312
ISBN-13 978-620-2-00431-2 / 9786202004312
Zustand Neuware
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