[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.163.159.27. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
October 1977

Chondrodysplasia PunctataConradi-Hünermann Syndrome

Author Affiliations

From the Divisions of Dermatology and Immunology, Department of Pediatrics, and the Division of Dermatology, Department of Medicine, Michael Reese Hospital and Medical Center, Chicago.

Arch Dermatol. 1977;113(10):1431-1434. doi:10.1001/archderm.1977.01640100109022
Abstract

• A 10-day-old girl was examined because of a peculiar, patterned hyperkeratosis that was noted at birth. The lesions were distributed over the trunk and limbs and consisted of whorls and streaks of thick, yellow, adherent scales. The salient histologic feature was marked hyperkeratosis with deep invagination of the dilated pilosebaceous ostia nearly to the level of the hair bulb. Additional physical abnormalities included patchy alopecia, bilateral zonular cataracts, a depressed nasal bridge, small stature, and multiple skeletal deformities. Roentgenograms demonstrated widespread stippled epiphyses characteristic of ConradiHünermann syndrome.

(Arch Dermatol 113:1431-1434, 1977)

×