Acquired bilateral longitudinal true leukonychia in a 35-year-old woman
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چکیده
منابع مشابه
acquired bilateral longitudinal true leukonychia in a 35‑year‑old woman
acquired bilateral longitudinal true leukonychia is a rare disorder. we present a case of a 35‑year‑old healthy woman presented with this unusual and rare manifestation. she mentioned a history of unprotected exposure to detergents and bleaching chemical agents. considering her low zinc level, she was prescribed with zinc capsules and recommended to avoid chemical substances for 6 months. durin...
متن کاملAcquired Bilateral Longitudinal True Leukonychia in a 35-year-old Woman
Acquired bilateral longitudinal true leukonychia is a rare disorder. We present a case of a 35-year-old healthy woman presented with this unusual and rare manifestation. She mentioned a history of unprotected exposure to detergents and bleaching chemical agents. Considering her low zinc level, she was prescribed with zinc capsules and recommended to avoid chemical substances for 6 months. Durin...
متن کاملIdiopathic Acquired Leukonychia in a 34-Year-Old Patient
We present a rare case of a 34-year-old patient with persistent, progressive, acquired leukonychia totalis and partialis. Idiopathic acquired leukonychia is a rare chromatic disorder of the nail not associated with other abnormalities and discernible etiology. Our case report did not link the inheritance of leukonychia with diverse clinical syndromes. To our knowledge, only five cases of idiopa...
متن کاملIdiopathic Acquired True Leukonychia Totalis and Partialis
262 Ann Dermatol Received Setember 21, 2012, Revised February 21, 2013, Accepted for publication April 22, 2013 Corresponding author: Sook-Ja Son, Department of Dermatology, Eulji General Hospital, 68 Hangeulbiseong-ro, Nowon-gu, Seoul 139-711, Korea. Tel: 82-2-970-8580, Fax: 82-2-974-1577, E-mail: ssjmdderma@ daum.net This is an Open Access article distributed under the terms of the Creative C...
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ژورنال
عنوان ژورنال: International Journal of Preventive Medicine
سال: 2016
ISSN: 2008-7802
DOI: 10.4103/2008-7802.193093