Helen Ollendorff Curth and Curth-Macklin Syndrome

Al Aboud, Khalid; Al Aboud, Daifullah

Helen Ollendorff Curth and Curth-Macklin Syndrome

Khalid Al Aboud^{*, 1}, Daifullah Al Aboud²

¹ Dermatology Department, King Faisal Hospital, Makkah, Saudi Arabia

² Dermatology Department, Taif University, Taif, Saudi Arabia

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Identifiers and Pagination:

Year: 2011
Volume: 5
First Page: 28
Last Page: 30
Publisher ID: TODJ-5-28
DOI: 10.2174/1874372201105010028

Article History:

Received Date: 18/07/2011
Revision Received Date: 06/10/2011
Acceptance Date: 06/10/2011
Electronic publication date: 10/11/2011
Collection year: 2011

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© 2011 Al Aboud and Al Aboud

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

^* Address correspondence to this author at the Dermatology Department, King Faisal Hospital, P.O Box 5440, Makkah 21955, Saudi Arabia; Tel: +966 2 5566411, Ext. 1110; Fax: +966 2 5563523; E-mail amoa65@hotmail.com

Helen Ollendorff Curth (1899-1982), is one of the pioneers in dermatology. In 1954, she and Madge Thurlow Macklin (1893–1962), an American medical geneticist, reported, a rare congenital genodermatosis that was later known as Curth-Macklin syndrome. This syndrome is a rare autosomal dominant skin disorder characterized by extensive hyperkeratosis and palmo-plantar keratoderma.

Keywords: Dermatology, ichthyosis, skin.

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RESEARCH ARTICLE

Helen Ollendorff Curth and Curth-Macklin Syndrome

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