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HEREDITARY ANHIDROTIC ECTODERMAL DYSPLASIAA Clinical and Pathologic Study
BETTE Y. UPSHAW, M.D.;
HAMILTON MONTGOMERY, M.D.
Arch Derm Syphilol. 1949;60(6):1170-1183.
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THE SYNDROME of hereditary anhidrotic ectodermal dysplasia, which has as its most prominent characteristics anhidrosis, hypodontia or anodontia and hypotrichosis, is one of a group of approximately 200 primarily cutaneous congenital abnormalities that are described in Cockayne's1 extensive study of this subject. Of this group, the following five types of abnormalities were studied and described by one of us (B. Y. U.) in a Mayo Foundation thesis, "Congenital Ectodermal and Mesodermal Dysplasias; A Clinical and Pathological Study": (1) anhidrotic ectodermal dysplasia, (2) hidrotic ectodermal dysplasia, (3) erythroderma ichthysiforme, (4) pachyonychia congenita and (5) Ehlers-Danlos syndrome.
In our experience, each and all of these five types of abnormalities can well be called rare; less than 40 patients affected by them have been encountered at the Mayo Clinic in the past twenty-seven years. This paper will be confined to the study of the 4 patients affected by anhidrotic ectodermal
. . . [Full Text PDF of this Article]
Author Affiliations
Fellow in Dermatology and Syphilology, Mayo Foundation; ROCHESTER, MINN.
From the section on Dermatology and Syphilology, Mayo Clinic.
Footnotes
Abridgment of a thesis submitted by Dr. Upshaw to the Faculty of the Graduate School of the University of Minnesota in partial fulfilment of the requirements for the degree of Master of Science in Dermatology.
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