Incoming and outgoing links Kindler syndrome
Back to articleIncoming links
- Brain syndrome
- Dental diseases, skin changes
- FERMT1 Gene
- Kindlin-1
- Marghescu-brown falco syndrome
- PID
- Poikiloderma, congenital with warty hyperkeratosis
- Poikiloderma, hereditary acrokeratotic, kindler type
- Poikiloderma, hereditary acrokeratotic, type weary
- Poikiloderma, hereditary with sclerotherapy
- Quinolinol sulphate monohydrate solution 0,1 % (nrf 11.127.)
- Reticular hyperpigmentations
- Thomson syndrome
- Weary-kindler, m.
Outgoing links
- Cytoskeleton
- Dyskeratosis congenita
- Epidermolysis bullosa hereditaria (overview)
- FERMT1 Gene
- Glucorticosteroids topical
- Hyperkeratoses
- Poikiloderma, hereditary with sclerotherapy
- Potassium permanganate
- Pruritus
- Tgf-beta
- Triamcinolone acetonide cream hydrophilic 0,025/0,05/0,1% (nrf 11.38.)
- Wound treatment