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Genodermatosen
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Genodermatosen
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| You are here: Genodermatosen | ||
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20.2.2 Ichthyosen | ||
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20.2.2.4 kongenitale Ichthyosen | ||
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20.2.3 Follikuläre Keratosen | ||
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20.2.3.2 Keratosis pilaris atrophicans (Ulerythema ophryoges) | ||
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20.2.4 Sonstige angeborene Verhornungsstörungen | ||
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20.2.4.1 Pemphigus chronicus benignus familiaris (M. Hailey-Hailey) | ||
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20.2.4.2 Erythrokeratodermien | ||
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20.2.4.4 Hyperkeratosis lenticularis perstans | ||
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20.2.5 Palmoplantarkeratosen | ||
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20.2.5.2 Keratosis palmoplantaris diffusa (rudiment) | ||
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20.2.6 Streifenförmige Hautveränderungen | ||
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20.2.6.2 Incontinentia pigmenti achromians | ||
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20.2.6.3 Aplasia cutis congenita | ||
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20.2.6.5 ILVEN-Nävus | ||
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20.2.6.6 Schimmelpennig-Feuerstein-Mims-Syndrom (in submission) | ||
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20.2.7 Ektodermale Dysplasien | ||
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20.2.8 Erbliche bullöse Krankheiten | ||
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20.2.8.1 Epidermolysis bullosa (rudiment) | ||
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20.2.9 Erkrankungen des Bindegewebes | ||
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20.2.9.1 Lipoidproteinose | ||
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20.2.9.3 Fokale dermale Hypoplasie | ||
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20.2.9.5 Cutis laxa | ||
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20.2.10 Poikilodermien | ||
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20.2.11 Genodermatosen mit Malignom-Assoziation | ||
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20.2.11.2 Carney-Syndrom | ||
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20.2.11.3 Cowden-Syndrom (rudiment) | ||
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20.2.11.4 Syndrom der dysplastischen Nävi | ||
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20.2.11.5 Gardner-Syndrom (rudiment) | ||
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20.2.11.6 Multiple endokrine Neoplasien Typ 2b | ||
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20.2.11.8 Torre-Muir-Syndrom (rudiment) | ||
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20.2.11.11 Bloom-Syndrom | ||
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20.2.11.13 Fanconi-Anämie | ||
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20.2.11.15 Werner-Syndrom (rudiment) | ||
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20.2.11.16 Xeroderma pigmentosa (rudiment) | ||
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Phakomatosen