Keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of unknown etiology in which increased susceptibility to viral, bacterial, and mycotic infections has been observed. We report an infant with KID syndrome who died from overwhelming systemic infection. To date, investigations into the immune function of patients with this syndrome have not revealed a common underlying systemic immune deficit. However, the severity of infections and multiplicity of organisms observed in this syndrome suggest that a primary immunodeficiency is present in addition to an impaired cutaneous barrier to microorganisms.
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Royal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
Muthiah, S.
Goodhead, C.
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Royal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
Goodhead, C.
Splitt, M.
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Ctr Life, Inst Human Genet, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
Splitt, M.
Fenton, A.
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Royal Victoria Infirm, Dept Neonatol, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
Fenton, A.
Leech, S.
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Royal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England
Leech, S.
Natarajan, S.
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Royal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, EnglandRoyal Victoria Infirm, Dept Dermatol, Newcastle Upon Tyne, Tyne & Wear, England