Verweise von und zu Ichthyosis (overview)
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- Acitretin
- Acrodermatitis enteropathica
- Acanthosis
- ALOXE3 Gene
- Anhidrotic ectodermal dysplasia
- CYP4F22-Related Autosomal Recessive Congenital Ichthyosis
- Ichthyosis lamellosa and congenital (with preserved transglutaminase activity)
- Chondrodysplasia calcificans congenita
- Comel-netherton syndrome
- CYP4F22 Gene
- Diogenes symptom complex
- Down syndrome
- Dystrophia myotonica
- Epidermolytic ichthyosis
- Erythrokeratodermia progressive, type burns
- Harlequin-ichthyosis
- Hypohidrosis
- Ichthyosis, therapy
- Ichthyosis congenita
- Ichthyosis hand, or foot
- Ichthyosis hystrix
- Ichthyosis, paraneoplastic
- Ichthyosis simplex
- Keratin
- Keratosis palmoplantaris with mutations in connexin 26
- Collodion baby
- KRT1 Gene
- NIPAL4 Gene
- Oligohidrosis
- Onychogrypose
- Paraffins
- Pibi(d)s syndrome
- Pseudoichthyoses
- Refsum syndrome
- Rehabilitation, dermatological
- Salicylic acid
- Sebostasis
- Sjögren-larsson syndrome
- Brine bath
- STIM1 Gene
- Multiple sulphatase deficiency
- Superficial epidermolytic ichthyosis
- Gluten-Related Dermatological Disorders
Verweise zu anderen Artikeln
- ABCA12 Gene
- ALOX12B Gene
- ALOXE3 Gene
- Anular epidermolytic ichthyosis
- Atrichia congenita with horny cysts
- Autosomal recessive congenital ichthyosis
- Autosomal recessive congenital ichthyosis with mutation in TGM1
- Bathing suit ichthyosis
- CASP14 Gene
- CDSN Gene
- CERS3 Gene
- Child syndrome
- Chondrodysplasia calcificans congenita
- Comel-netherton syndrome
- CYP4F22 Gene
- Dorfman-chanarin syndrome
- ELOVL4 gene
- Epidermolytic ichthyosis
- Erythrokeratodermia figurata variabilis
- Erythrokeratoderma (overview)
- FLG Gene
- GJB4 Gene
- Harlequin-ichthyosis
- Ichthyosis, therapy
- Ichthyosis, spastic quadriplegia, and mental retardation
- Ichthyosis x-linked recessive
- Ichthyosis acquisita (pseudoichthyosis)
- Ichthyosis curth-macklin
- Ichthyosis vulgaris
- Keratosis linearis-ichthyosis congenita-keratoderma with mutations in pomp
- Keratosis palmoplantaris with mutations in connexin 26
- Loricrin keratoderm
- Congenital reticular ichthyosiform erythroderma
- KRT10 Gene
- KRT1 Gene
- KRT2 Gene
- LIPN Gene
- LOR Gene
- Netherton syndrome
- NIPAL4 Gene
- Palmoplantar keratoses (overview)
- Peeling skin syndrome
- PNPLA1 Gene
- POMP gene
- Refsum syndrome
- Self-improving congenital ichthyosis
- SERPINB8 Gene
- Sjögren-larsson syndrome
- ST14 Gene
- STS Gene
- Superficial epidermolytic ichthyosis
- TGM1 GenE
- Trichothiodystrophy