Female, 27
This is a Haematogenic Iris Constitution, subtype by Neurogenic disposition. Could you explain it genetic traits and common weakness characteristics ? Actually, if we want to know more about her genetic weaknesses, the most accurate and precise method is to analyse it IPB structure and morphologies. This is not a modern & advanced iris analysis technique but a basic and compulsory requirement for modern Iridologist to practice ! Please see below IPB illustrations, What can it tell you about her genetic predisposition and family medical history ? Could you find it at pupillary & ciliary zones ? If we are not familiar with the IPB analysis, this iris has limited genetic information / signs to retrieve. In addition, you could only find some iris signs attached on the ciliary zones, that I would consider less important and could not be sufficiently represent a core or major genetic deficiency for this person. I would suggest most of the important iris signs - 80% is attached on inner pupillary border tissues & pupillary zone, remaining of 20% is attached on the external border of the collarette to ciliary zone. So, what is your rules ? where you place for your attention on 80% Vs 20% ?
a), c) & d) is squared IPB, obviously it indicate a family medical history of thyroid dysfunction.
b) A unique IPB of "S' sign, it is a solitary and tend to appear in the frontal aspect of the IPB. It indicate a Prolactin disturbances, further explanation please refer to John Andrews textbook on IPB topic.
e) Crypts located on ciliary zone - 190', 338' & 25' at topographical areas of kidneys, frontal sinus and cerebellum.
In general, the Squared & S sign IPB is the most important and significant iris sign on this iris sample.
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