FRANCIS E. BRUNO, M.D.; HUGO T. ENGELHARDT, M.D.
This content is PDF only. Please click on the PDF icon to access.
Recently we have had occasion to observe a family which exhibited some of the clinical characteristics of hereditary ectodermal dysplasia. These characteristics have been described in detail by other authors.1, 2, 3, 4, 5, 6, 7, 8, 9 Therefore, we wish to limit this presentation to case reports and a brief discussion of this interesting and rare anomaly. Of this family of seven children, four manifested definite evidences of this defect.
Case 1. Mrs. R. D. P., aged 25, a white female, was admitted to the Department of Medicine, Hutchinson Memorial Clinic on October 24, 1941. The chief
BRUNO FE, ENGELHARDT HT. HEREDITARY ECTODERMAL DYSPLASIA1. Ann Intern Med. 1944;20:140–144. doi: 10.7326/0003-4819-20-1-140
Download citation file:
Published: Ann Intern Med. 1944;20(1):140-144.
Results provided by:
Copyright © 2019 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use