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Multiple lentigines syndrome - Overview

Alternative Names

Leopard syndrome

Definition of Multiple lentigines syndrome:

Multiple lentigines syndrome is an inherited disorder identified by an increased number of lentigines (freckle-like spots).

Causes, incidence, and risk factors:

Multiple lentigines syndrome is inherited as an autosomal dominant trait. People with this condition have large numbers of lentigines. Lentigines are skin markings that are somewhat darker than true freckles. They are present from birth. They are located mostly on the trunk and neck.

  • Reviewed last on: 5/13/2011
  • Jonathan Kantor, MD, North Florida Dermatology Associates, Jacksonville, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

References

Gibbs NF, Makkar HS. Disorders of Hyperpigmentation and Melanocytes. In: Eichenfield LF, Frieden IJ, Esterly NB, eds. Textbook of Neonatal Dermatology. 2nd Ed. Philadelphia, Pa: Saunders Elsevier; 2001: p. 196.

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