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Up to: Hereditary skin disorder · Constitutional neutropenia · Hereditary poikiloderma
Poikiloderma with neutropenia
A skin disease characterized by poikiloderma, hyperkeratotic nails, generalized hyperkeratosis on palms and soles, neutropenia, short stature, and recurrent pulmonary infections. It has material basis in mutation in the C16ORF57 gene on chromosome 16q13.
This condition has no sub-types.