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Verweise von und zu Epidermolysis bullosa hereditaria (overview)

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  • Acrodermatitis enteropathica
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  • Dystrophia bullosa hereditaria - type maculatus seu amsterdam
  • Epidermolysis
  • Epidermolysis bullosa
  • Epidermolysis bullosa dystrophica dominans, generalized
  • Dystrophic epidermolysis bullosa inversa
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  • Epidermolysis bullosa dystrophica recessive, severe generalized
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  • Epidermolysis bullosa junctionalis with hypacusis
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  • Epidermolysis bullosa simplex with muscular dystrophy an mutation in PLEC
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  • Incontinentia pigmenti (Bloch-Sulzberger)
  • Isolated toenail dystrophy
  • Kindler syndrome
  • KLHL24 Gene
  • Onychodysplasia congenital of the index finger
  • Pachyonychia congenita
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  • Plectin
  • Porphyria cutanea tarda
  • Porphyria erythropoetica congenita
  • Rehabilitation, dermatological
  • Back mutation
  • TGM5 Gene
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  • Urticaria pigmentosa bullosa
  • Dental diseases, skin changes
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  • Acrodermatitis enteropathica
  • Epidermolysis bullosa, lethal acantholytic
  • Acral peeling skin syndrome
  • Antibiogram
  • Antibiotics
  • Aplasia cutis congenita (overview)
  • Basal membrane
  • Transient bullous dermolysis of the newborn
  • Bullous Pemphigoid
  • Candidoses
  • COL7A1 Gene
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  • DSP Gene
  • DST Gene
  • Ectodermal dysplasia-skin fragility syndrome
  • Ema
  • Epidermolysis bullosa acquisita
  • Epidermolysis bullosa dystrophica albopapuloida
  • Epidermolysis bullosa with congenital abscence of the skin and deformity of nails
  • Epidermolysis bullosa dystrophica dominans, generalized
  • Dystrophic epidermolysis bullosa inversa
  • Epidermolysis bullosa dystrophica praetibialis
  • Pretibial dystrophic epidermolysis bullosa, recessive
  • Dystrophic epidermolysis bullosa pruriginosa recessive
  • Epidermolysis bullosa dystrophica recessive non-hallopeau-siemens
  • Epidermolysis bullosa dystrophica recessive, severe generalized
  • Epidermolysis bullosa junctionalis generalized intermediaries (non-herlitz)
  • Epidermolysis bullosa junctionalis, generalized severe (historical: Herlitz type)
  • Epidermolysis bullosa junctionalis with hypacusis
  • Interstitial lung disease , nephrotic syndrome and integrin alpha-3 Mutation
  • Epidermolysis bullosa junctionalis with pyloric atresia
  • Epidermolysis Bullosa Simplex 3, Localized or Generalized Intermediate, with Bp230 Deficiency (EBS3)
  • Epidermolysis bullosa simplex, localized or generalized intermediate, with mutation in EXPH5
  • Epidermolysis bullosa simplex 3, basal, autosomal recessive, with bp230 deficiency
  • Epidermolysis bullosa simplex generalized intermediaries (köbner)
  • Epidermolysis bullosa simplex generalized severe (dowling-meara)
  • Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
  • Epidermolysis bullosa simplex localized (Weber-Cockayne)
  • Epidermolysis Bullosa Simplex with KLHL24 Mutations
  • Epidermolysis bullosa simplex with mottled pigmentation
  • Epidermolysis bullosa simplex with muscular dystrophy an mutation in PLEC
  • Epidermolysis bullosa simplex mit Mutation in Plectin-Isoform 1a
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  • EXPH5 Gene
  • Glucorticosteroids topical
  • Urea (overview)
  • Skin fragility-woolly hair syndrome
  • Herpes simplex virus infections
  • Contagious impetigo
  • Isolated toenail dystrophy
  • ITGB4 Gene
  • Potassium permanganate
  • Kindler syndrome
  • KLHL24 Gene
  • KRT14 Gene
  • KRT5 Gene
  • LAMA3 Gene
  • Laryngo-onycho-cutaneous-syndrome
  • Linear IgA dermatosis
  • Mastocytosis (overview)
  • Orphan diseases
  • Peeling skin syndrome
  • Pemphigus diseases (overview)
  • Pigment incontinence
  • PKP1 Gene
  • PLEC Gene
  • Polihexanide
  • Porphyria (overview)
  • Pruritus
  • Staphylococcal scalded skin syndrome
  • TGM5 Gene
  • Thymic stromal lymphopoietin
  • Triamcinolone acetonide
  • Wound treatment
  • Cytoskeleton
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