The Association of Sarcoidosis, Erythema Nodosum, and Arthritis.
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Adult↗
Biomedical subjects
C H Behlen
Publications and source records attributed to C H Behlen.
Unusual familial hypopigmentary anomaly.
A hitherto unreported bilateral and symmetrical hypopigmentary anomaly is reported in five members of a Negro family. The pattern of inheritance would appear to be autosomal dominant and it is concluded that this is a benign pigmentary alteration unrelated to underlying disease.
Adolescent↗
Benign mucous membrane pemphigus with a generalized eruption.
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Eye Diseases↗