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Sebaceous Gland Papules in Anhidrotic Ectodermal Dysplasia
Stephen I. Katz, MD;
Neal S. Penneys, MD
Arch Dermatol. 1971;103(5):507-509.
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).
Author Affiliations
Miami, Fla
From the Department of Dermatology, University of Miami (Fla) School of Medicine. Dr. Katz is now with the Department of Dermatology, Walter Reed General Hospital, Washington, DC.
Footnotes
Accepted for publication Nov 7, 1970.
Reprint requests to Department of Dermatology, University of Miami Medical School, Miami, Fla 33136 (Dr. Penneys).
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