Related Experiment Video
Updated: Jan 25, 2026

Reverse Genetic Approach to Identify Regulators of Pigmentation using Zebrafish
Published on: March 1, 2022
[Pigmented macules as possible early signs of genetic syndromes]
H Hamm1, K Emmerich2, J Olk2
1Klinik und Poliklinik für Dermatologie, Venerologie und Allergologie, Universitätsklinikum Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Deutschland. hamm_h@ukw.de.
Abstract:
Solitary congenital or early apparent pigmented macules are usually without relevance; however, when multiple, extensive or in a patterned arrangement, they are not uncommonly the first sign of an underlying genetic syndrome. The present article gives an overview on the clinical significance of multiple café-au-lait macules, multiple lentigines and pigmentary mosaicism and discusses the differential diagnosis of associated syndromes. Early diagnosis with the essential contribution of the dermatologist is not only important for genetic counseling but can also contribute to avoidance of sometimes life-threatening complications.
Related Concept Videos
Signs of Puberty
Introduction to the Sign Test
Sign Convention
The normal force acts perpendicular to the beam's cross-section and can...
Sign Test for Nominal Data
For example, consider a...
Introduction to Vital Signs
Vital signs help healthcare professionals assess an individual's well-being and detect any functional changes...
Sign Test for Matched Pairs
To conduct the sign test, we first calculate the differences in...

