4.3 Editorial Material

Cafe au Lait Macules and Associated Genetic Syndromes

Journal

JOURNAL OF PEDIATRIC HEALTH CARE
Volume 34, Issue 1, Pages 71-81

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.pedhc.2019.05.001

Keywords

Cafe au lait macule; neurofibromatosis type 1; Legius syndrome; McCune-Albright syndrome; Noonan syndrome with multiple lentigines

Ask authors/readers for more resources

Cafe au lait macules (CALMs) are a common, isolated dermatologic finding in the general population. But when do these irregularly shaped, jagged-edged, flat, hyperpigmented birthmarks suggest something that may warrant referral? Most pediatric providers are familiar with the association of CALMs and neurofibromatosis type 1. There are, however, other genetic conditions associated with these seemingly benign skin spots. This article provides an overview of CALMs, followed by a summary of several conditions associated with CALMs ranging from the most common (neurofibromatosis type 1) to rare, ring chromosome syndromes. It reviews the associated gene(s), pattern of inheritance, incidence, presenting symptoms, diagnosis, and management for these genetic conditions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available