Idiopathic Acquired Leukonychia in a 34-Year-Old Patient

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Idiopathic 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...

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Idiopathic 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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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...

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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...

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Intrathoracic mass in a 34 year old cystic fibrosis patient.

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ژورنال

عنوان ژورنال: Case Reports in Medicine

سال: 2009

ISSN: 1687-9627,1687-9635

DOI: 10.1155/2009/495809