A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis
About this course
- Released:
- Expires: August 18, 2028
Target Audience
This activity is intended for practicing dermatologists and other physicians involved in the treatment and management of diseases of the skin.
Learning Objective
To demonstrate the phenotypic variability associated with mutations in the gene encoding lanosterol synthase.
Accreditation and Designation Statement
Once the test is passed, a certificate of completion will be generated. The learning activity can be added to the Royal College of Physicians' CPD diary as a self-certified entry.
Activity Disclosures
No commercial support has been accepted related to the development or publication of this activity.