Indian Journal of Dermatology
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Year : 2022  |  Volume : 67  |  Issue : 2  |  Page : 161-163

Doors syndrome: Case report

1 From the Department of Dermatology, Famagusta State Hospital, Famagusta, Cyprus
2 Department of Otorhinolarngology, Famagusta State Hospital, Famagusta, Cyprus

Correspondence Address:
Dua Cebeci
Salamis Caddesi No 19, Famagusta
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijd.ijd_676_21

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DOORS syndrome is an autosomal recessive genetic neurometabolic disorder. It occurs equally in men and women. Major causes include TBC1D 24 mutations and genetic factors. Here, we discuss a 23-year-old male patient who applied to our clinic with anonychia of the toes and was diagnosed with DOORS syndrome with other accompanying clinical symptoms.

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