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Kniha Ectodermal Dysplasia -An Overview Mudit Agarwal

Ectodermal Dysplasia -An Overview

Autor: Mudit Agarwal, R. Sivasankary
Jazyk: Angličtina
Väzba: Brožovaná
Vydavateľ: LAP LAMBERT Academic Publishing
Dostupnosť: Skladom u dodávateľa
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Ectodermal dysplasia (ED) refers to a heterogeneous group of inherited disorders characterized by ab...

Informácie o knihe

Autor
Mudit Agarwal, R. Sivasankary
Jazyk
Angličtina
Väzba
Kniha - Brožovaná
Vydalo
2025
Stránok
68
EAN
9786208010256
ISBN
620801025X
Enbook ID
49695999
Vydavateľ
LAP LAMBERT Academic Publishing
Hmotnosť
119
Rozmery
150 x 220 x 5

Kompletný popis

Ectodermal dysplasia (ED) refers to a heterogeneous group of inherited disorders characterized by abnormalities in two or more structures derived from the embryonic ectoderm, primarily affecting the skin, hair, nails, teeth, and sweat glands. The condition results from mutations in various genes, most commonly EDA, EDAR, and TP63, with inheritance patterns that include X-linked, autosomal dominant, and autosomal recessive forms. Clinically, affected individuals may present with sparse hair (hypotrichosis), missing or misshapen teeth (hypodontia or anodontia), reduced ability to sweat (hypohidrosis), and distinctive facial features. Diagnosis is based on clinical evaluation, family history, and genetic testing. There is no cure, and management is multidisciplinary, focusing on symptom relief, dental rehabilitation, temperature regulation, and psychosocial support. Advances in genetic research and prenatal diagnostics are improving early detection and opening avenues for potential gene-based therapies. Understanding the molecular basis of ED enhances both prognosis and the development of targeted interventions.

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