Adermatoglyphia Informative Speech

I will be informing you on a genetic disorder called Adermatoglyphia or other wise known as immigration delayed disorder.
The phenotypic display of Adermatoglyphia is the lack of fingerprints, and a thickening of the skin,and problems with nail formation. One other affect is the minor reduction in the ability to sweat.
Adermatoglyphia can be diagnosed but just looking at your hands,(go on look). However how often do you think about your fingerprints. If others in your family seem to have no fingerprints and your hands look similar to them and feel similar, then you to properly don't have fingerprints as well.
People with Adermatoglyphia have to go through more steps to leave or enter a country. They also struggle to live in warmer climates due to the reduced capability to sweat.
And was stopped by border control for she had no fingerprints, they were baffled so they contacted Peter Itan and Eli Spencer (of Tel Aviv University's Sackler Faculty of Medicine and the Tel Aviv Sourasky Medical Center) to do research on why she had none, they came up empty handed on the gene responsible. In 2011 a grad student found the gene responsible SMARCAD1.
SMARCAD1 gene's normal function is to provide instructions for make two versions of the SMARCAD1 protein: a full-length isoform that's job is to maintain the stability of cell's genetic information, and a skin-specific isoform. SMARCAD1 gene is located in (long Arm) at (chromosome) 4 (region) 2 (band) 2. (sub-band) 3, or