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Atlas of common and rare genodermatoses

Record Type:	Electronic resources : Monograph/item
Title/Author:	Atlas of common and rare genodermatosesby Nayera Moftah ... [et al.].
other author:	Moftah, Nayera.
Published:	Cham :Springer Nature Switzerland :2024.
Description:	xiv, 265 p. :ill. (chiefly color), digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	SkinAtlases.Diseases
Online resource:	https://doi.org/10.1007/978-3-031-60788-2
ISBN:	9783031607882$q(electronic bk.)

Atlas of common and rare genodermatoses
Atlas of common and rare genodermatoses[electronic resource] /by Nayera Moftah ... [et al.]. - Cham :Springer Nature Switzerland :2024. - xiv, 265 p. :ill. (chiefly color), digital ;24 cm.

Preface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.

The management of cutaneous findings in genodermatoses is challenging to the practicing clinician, especially when all hues of skin and skin types are contemplated, and first-line therapies often inadequate. This carefully crafted Atlas includes all sorts of different ethnic skin types, while featuring a wealth of over 1000 commented images collected in more than a decade, including 200 rare genodermatoses, and providing the reader with key points for correct dermatological diagnosis. The contents start with disorders of keratinization and pigmentation, as well as bullous, acantholytic, dermal, hair and nail diseases. Successively, immunodeficiency syndromes and their skin related symptoms, hamartoneoplastic syndromes and defective excision repair syndromes are presented. The addition of vascular disorders, as well as syndromes with premature aging grant full topic coverage. This Atlas of Common and Rare Genodermatoses will be a valued companion to dermatologists and paediatric specialists in their daily practice.

ISBN: 9783031607882$q(electronic bk.)

Standard No.: 10.1007/978-3-031-60788-2doiSubjects--Topical Terms:

984500
Skin
--Diseases--Atlases.

LC Class. No.: RL793

Dewey Class. No.: 616.5042

Atlas of common and rare genodermatoses
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300 $a xiv, 265 p. : $b ill. (chiefly color), digital ; $c 24 cm.
505 0 $a Preface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.
520 $a The management of cutaneous findings in genodermatoses is challenging to the practicing clinician, especially when all hues of skin and skin types are contemplated, and first-line therapies often inadequate. This carefully crafted Atlas includes all sorts of different ethnic skin types, while featuring a wealth of over 1000 commented images collected in more than a decade, including 200 rare genodermatoses, and providing the reader with key points for correct dermatological diagnosis. The contents start with disorders of keratinization and pigmentation, as well as bullous, acantholytic, dermal, hair and nail diseases. Successively, immunodeficiency syndromes and their skin related symptoms, hamartoneoplastic syndromes and defective excision repair syndromes are presented. The addition of vascular disorders, as well as syndromes with premature aging grant full topic coverage. This Atlas of Common and Rare Genodermatoses will be a valued companion to dermatologists and paediatric specialists in their daily practice.
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650 2 4 $a Diagnosis. $3 192756
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