This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

LI (lamellar ichthyosis)

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

  • lamellar ichthyosis is inherited as an autosomal recessive with an estimated incidence of less than 1 per 300,000
  • usually it starts at birth or within the first 3 months. It begins as a generalised erythema and subsequently the skin becomes thickened and scaly. The entire cutaneous area may become scaly - including flexures, palms and soles
  • the scales are large and parchment-like. They may be verrucous especially around the joints
  • additional features in some patients include palmoplantar hyperkeratosis, ectropion and scarring alopecia
  • sweating may be abnormal and the patient hyperpyrexial. Skin infections are common
  • the genetic mutation causing lamellar ichthyosis is, at present, unknown

It may present as a "collodion baby" - premature, and with shiny skin which feels hard and rigid.


Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.