Peculiarly, parents of patients with the syndrome experienced difficulties conceiving both children with Hänensen and other conditions unrelated to the syndrome at a rate higher than the general population. Studies suggest the genetic basis for the disorder lies within a shared genetic heritage related to the shallow pools and low-lying areas surrounding the area affected.
Clinical observations suggested no distinct disorder features in any of the patients surveyed. Since affected individuals and their relatives exhibited no other congenital abnormalities, oral examinations, analysis, revealed unusual fears and more suspicious behavior than normal individuals when asked about their feelings. It was determined that all exposed children had a severe fear of change.
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