[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.167.149.128. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
March 1972

Lamellar Ichthyosis of the NewbornA Distinct Clinical Entity: Its Comparison to the Other Ichthyosiform Erythrodermas

Author Affiliations

Burbank, Calif; San Francisco; Albuquerque, NM; Portland, Ore; San Francisco

From the departments of dermatology, University of California, Irvine (Dr. Reed) and San Francisco (Drs. Herwick and Conant); Winrock Medical Center, Albuquerque, NM (Dr. Har-; ville); and the University of Oregon Medical School, Portland (Dr. Porter).

Arch Dermatol. 1972;105(3):394-399. doi:10.1001/archderm.1972.01620060036006
Abstract

Lamellar ichthyosis of the newborn is a distinct genetic entity, probably autosomal recessive in inheritance. Babies born with this condition are covered with a collodion-like membrane, but the skin clears almost completely in the first months of life and they remain free of ichthyosis. Two brothers had lamellar ichthyosis of the newborn, and a similar child subsequently developed cataracts and other abnormalities. None of these three patients had stippled epiphyses. A fourth patient, a child with classical Conradi's disease (stippled epiphyses and cataracts) had erythroderma at birth. This cleared completely in a few months, but other skin and hair abnormalities have persisted.

×