Name: Ectodermal Dysplasia -An Overview (en Inglés)
SKU: 66204846
Price: 62.06 USD
Availability: InStock
Author: Muthunagai, R.; Agarwal, Mudit; Sivasankary, R.

portada Ectodermal Dysplasia -An Overview (en Inglés)

Ectodermal Dysplasia -An Overview (en Inglés)

Formato

Libro Físico

Editorial

LAP Lambert Academic Publishing

Autor

Muthunagai, R.; Agarwal, Mudit; Sivasankary, R.

Idioma

Inglés

N° páginas

Encuadernación

Tapa Blanda

Dimensiones

22.9x15.2x0.4 cm

ISBN13

9786208010256

Ectodermal Dysplasia -An Overview (en Inglés)

Muthunagai, R.; Agarwal, Mudit; Sivasankary, R. (Autor) · LAP Lambert Academic Publishing · Tapa Blanda

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Reseña del libro "Ectodermal Dysplasia -An Overview (en Inglés)"

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.