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Version October 2024
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Autosomal recessive congenital ichthyoses
Birt-Hogg-Dubé syndrome
Brooke-Spiegler syndrome (<i>CYLD</i> cutaneous syndrome)
Buschke-Ollendorff syndrome
Carney complex
Cutis verticis gyrata
Darier disease
Diagnosis of epidermolysis bullosa
Ectodermal dysplasias
Epidermodysplasia verruciformis
Epidermolysis bullosa: Epidemiology, pathogenesis, classification, and clinical features
Focal dermal hypoplasia (Goltz syndrome)
Hailey-Hailey disease (benign familial pemphigus)
Hereditary leiomyomatosis and renal cell cancer (HLRCC)
Hermansky-Pudlak syndrome
Hutchinson-Gilford progeria syndrome
Ichthyosis vulgaris
Incontinentia pigmenti
Inherited ichthyosis: Overview of management
Keratinopathic ichthyoses
Kindler epidermolysis bullosa
Lipoid proteinosis
Muir-Torre syndrome
Nail disorders in children: Congenital and hereditary nail diseases
Netherton syndrome
Nevoid basal cell carcinoma syndrome (Gorlin syndrome)
Oculocutaneous albinism
Overview and classification of the inherited ichthyoses
Overview of the management of epidermolysis bullosa
Pachyonychia congenita
Palmoplantar keratoderma
Peeling skin syndromes
Piebaldism
Pigmentary mosaicism (hypomelanosis of Ito)
Pseudoxanthoma elasticum
Stiff skin syndrome
The genodermatoses: An overview
The hereditary dyschromatoses
Tumor protein p63 (TP63)-related ectodermal dysplasias
Werner syndrome
Xeroderma pigmentosum
X-linked ichthyosis
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