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  Vol. 102 No. 6, December 1970 TABLE OF CONTENTS
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Pilosebaceous Dysplasia in the Oral-Facial-Digital Syndrome

Lawrence M. Solomon, MD; David Fretzin, MD; Samuel Pruzansky, DDS

Arch Dermatol. 1970;102(6):598-602.


Abstract

The clinical features of eight female patients with the oral-facial-digital (OFD) syndrome, including a description of the skin and its histological and pharmacological characteristics are described. The OFD syndrome is characterized in part by a cutaneous dyplasia which includes a marked diminution in sebaceous glands, some decrease in hair follicles, and early keratinous cyst formation, which may represent maldevelopment of the pilosebaceous unit.



Author Affiliations

Chicago

From the Department of Dermatology and Center for Cranio-facial Anomalies, colleges of medicine and dentistry, University of Illinois, Chicago.


Footnotes

Accepted for publication Aug 21, 1970.

Reprint requests to Department of Dermatology, College of Medicine, University of Illinois, 840 S Wood St, Chicago 60680 (Dr. Solomon).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Cutaneous Findings in Craniofacial Malformation Syndromes
Orlow
Arch Dermatol 1992;128:1379-1386.
ABSTRACT  

The Ectodermal Dysplasias: Problems of Classification and Some Newer Syndromes
Solomon and Keuer
Arch Dermatol 1980;116:1295-1299.
ABSTRACT  





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