Kindler syndrome
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.
Symptoms and signs
Infants and young children with Kindler syndrome have a tendency to blister with minor trauma and are prone to sunburns. [Source: Wikipedia 
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- Acrokeratotic poikiloderma
- Bullous acrokeratotic poikiloderma of Kindler and Weary
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Hereditary acrokeratotic poikiloderma
- Hereditary acrokeratotic poikiloderma of Kindler-Weary
- Hyperkeratosis-hyperpigmentation syndrome
- Weary-Kindler syndrome
