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Sebaceous Gland Papules in Anhidrotic Ectodermal Dysplasia

Sebaceous Gland Papules in Anhidrotic Ectodermal Dysplasia Abstract Six members of a family had various manifestations of the syndrome, anhidrotic ectodermal dysplasia; included in this family were identical twin boys with all the stigmas of this syndrome. In addition to the usual cutaneous changes associated with the syndrome, myriads of sebaceous gland papules were seen on the malar areas, nasolabial folds, and foreheads of the identical twins. The genetics of inheritance of this syndrome in this family conformed to that commonly accepted (X-linked recessive). References 1. Kerr CB, Wells RS, Cooper KE: Gene effect in carriers of anhidrotic ectodermal dysplasia . J Med Genet 3:169-176, 1966.Crossref 2. de Silva PCC: Hereditary ectodermal dysplasia of anhydrotic type . Quart J Med 8:97-113, 1939. 3. Goeckermann WH: Congenital ectodermal defect: With report of a case . Arch Derm Syph 1:396-412, 1920.Crossref 4. MacKee GM, Andrews GC: Congenital ectodermal defect . Arch Derm Syph 10:673-701, 1924.Crossref 5. Butterworth T, Strean LP: Clinical Genodermatology . Baltimore, Williams & Wilkins Co, 1962, pp 51-53. 6. De Mars R, Sarto G, Felex JS, et al: Lesch-Nyhan mutation: Prenatal detection and amniotic fluid cells . Science 164:1303-1305, 1969.Crossref 7. Sever RJ, Frost P, Weinstein G: Eye changes in ichthyosis . JAMA 206:2283-2286, 1968.Crossref http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Dermatology American Medical Association

Sebaceous Gland Papules in Anhidrotic Ectodermal Dysplasia

Archives of Dermatology , Volume 103 (5) – May 1, 1971

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Publisher
American Medical Association
Copyright
Copyright © 1971 American Medical Association. All Rights Reserved.
ISSN
0003-987X
eISSN
1538-3652
DOI
10.1001/archderm.1971.04000170041010
Publisher site
See Article on Publisher Site

Abstract

Abstract Six members of a family had various manifestations of the syndrome, anhidrotic ectodermal dysplasia; included in this family were identical twin boys with all the stigmas of this syndrome. In addition to the usual cutaneous changes associated with the syndrome, myriads of sebaceous gland papules were seen on the malar areas, nasolabial folds, and foreheads of the identical twins. The genetics of inheritance of this syndrome in this family conformed to that commonly accepted (X-linked recessive). References 1. Kerr CB, Wells RS, Cooper KE: Gene effect in carriers of anhidrotic ectodermal dysplasia . J Med Genet 3:169-176, 1966.Crossref 2. de Silva PCC: Hereditary ectodermal dysplasia of anhydrotic type . Quart J Med 8:97-113, 1939. 3. Goeckermann WH: Congenital ectodermal defect: With report of a case . Arch Derm Syph 1:396-412, 1920.Crossref 4. MacKee GM, Andrews GC: Congenital ectodermal defect . Arch Derm Syph 10:673-701, 1924.Crossref 5. Butterworth T, Strean LP: Clinical Genodermatology . Baltimore, Williams & Wilkins Co, 1962, pp 51-53. 6. De Mars R, Sarto G, Felex JS, et al: Lesch-Nyhan mutation: Prenatal detection and amniotic fluid cells . Science 164:1303-1305, 1969.Crossref 7. Sever RJ, Frost P, Weinstein G: Eye changes in ichthyosis . JAMA 206:2283-2286, 1968.Crossref

Journal

Archives of DermatologyAmerican Medical Association

Published: May 1, 1971

References