Vendeur : GreatBookPrices, Columbia, MD, Etats-Unis
Etat : New. N° de réf. du vendeur 51224128-n
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Vendeur : PBShop.store US, Wood Dale, IL, Etats-Unis
PAP. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. N° de réf. du vendeur L0-9786208010256
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Vendeur : PBShop.store UK, Fairford, GLOS, Royaume-Uni
PAP. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. N° de réf. du vendeur L0-9786208010256
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Vendeur : GreatBookPrices, Columbia, MD, Etats-Unis
Etat : As New. Unread book in perfect condition. N° de réf. du vendeur 51224128
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Vendeur : California Books, Miami, FL, Etats-Unis
Etat : New. N° de réf. du vendeur I-9786208010256
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Vendeur : GreatBookPricesUK, Woodford Green, Royaume-Uni
Etat : New. N° de réf. du vendeur 51224128-n
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Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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. 68 pp. Englisch. N° de réf. du vendeur 9786208010256
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Vendeur : GreatBookPricesUK, Woodford Green, Royaume-Uni
Etat : As New. Unread book in perfect condition. N° de réf. du vendeur 51224128
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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. N° de réf. du vendeur 9786208010256
Quantité disponible : 1 disponible(s)
Vendeur : Books Puddle, Woodside, NY, Etats-Unis
Etat : New. N° de réf. du vendeur 26405273487
Quantité disponible : 4 disponible(s)