All rights reserved.
All rights reserved.

Dermatoglyphics refers to the branch of science in the study of the patterns of skins (dermal) ridges
present on the fingers, toes and the soles of human. Its reveals the congenital links between our
fingers and our intrinsic qualities and talents. These patterns are formed from the external ectoderm
and usually occur during the fetal development stage, The humans fingerprints form are thus formed
from the 13th to 21st week. Medical experts and scientists thus discovered that the amount of brain
cells distributed in different parts of the brain helps us understand a person’s multiple intelligences
as well as his innate potential capabilities and personality. Our fingerprints reveal to us what we need
and how we learn, transforming our lives through a holistic education approaches.

Dermatoglyphics features -:

When the fetus is in the mother’s womb, the life area of the fetus’ brain is developed. From 0-3
years old, the emotional area develops rapidly. Between 4-8 years old, the thought function/area is
developed. Whereas, between 9-16 years old the mental/spiritual part gradually matures. Hence,
after 17 years, “want” and “do not want” become the brain’s main model of operation.

The human brain is like a computer, 0-3 is equivalent to the hardware phase, 4-8-year-old is
equivalent to the software phase, and above 9 years old is equivalent to the operational phase,
namely practice using the computer.Page Title
Uniqueness : There are no two identical
fingerprints. One’s 10 fingers are not the same .
dermatoglyphics style, striae height, density,
quantity and location of the point is not the same
for everyone. No individual has ever displayed
the same fingerprint from another digit even if
taken from the same hand. Invariance :The
raised pattern network of lifetime from birth to
death will not change even if it is due to the
regeneration of the labor dermatoglyphics style,
quantity and profile shape which is determined
the same later.

Hereditary According to science statistics,
immediate family members will be more or less
the same between the striae. Normal human cells
have 23 pairs of chromosomes. If the
chromosomes of the tree or structure are
changed, it will cause the corresponding striae
mutation. Therefore, the striae have inherited
the mutation.
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