Back to Search
Start Over
Café au lait spots: When and how to pursue their genetic origins
- Source :
- Clinics in Dermatology. 38:421-431
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- Café au lait spots are common birthmarks seen sporadically and in association with several genetic syndromes. Dermatologists are often asked to evaluate these birthmarks both by other physicians and by parents. In some cases, it is challenging to know when and how to pursue further evaluation. Diagnostic challenges may come in the form of the appearance of the individual lesions, areas and patterns of cutaneous involvement, and associated features (or lack thereof). In this review, we aim to clarify when and how to evaluate the child with multiple or patterned café au lait spots and to explain some emerging concepts in our understanding of the genetics of these lesions.
- Subjects :
- Male
medicine.medical_specialty
Neurofibromatosis 1
Genetic syndromes
Dermatology
Diagnosis, Differential
030207 dermatology & venereal diseases
03 medical and health sciences
0302 clinical medicine
Café au lait spot
medicine
Humans
Birthmark
Child
Skin pathology
Genetic Association Studies
Germ-Line Mutation
Adaptor Proteins, Signal Transducing
Skin
030203 arthritis & rheumatology
Neurofibromin 1
business.industry
Cafe-au-Lait Spots
Infant, Newborn
Infant
Skin Diseases, Genetic
Syndrome
Gene deletion
medicine.disease
Cutaneous Involvement
Child, Preschool
Female
medicine.symptom
business
Genetic diagnosis
Gene Deletion
Subjects
Details
- ISSN :
- 0738081X
- Volume :
- 38
- Database :
- OpenAIRE
- Journal :
- Clinics in Dermatology
- Accession number :
- edsair.doi.dedup.....49a8592c98d98966bd548ce9149aaa93
- Full Text :
- https://doi.org/10.1016/j.clindermatol.2020.03.005