Misdiagnosis for 1qh + 16qh

In Facebook or in the article entitled 1qh + 16qh, infertility and ICF syndrome, I have already shown how different diagnoses were made.

However, the specific question about immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF) here in the city of Dortmund should have led to a careful analysis, just as there was at the beginning in the human genetics department of a university clinic in central Germany, at my place of work and second home at the time, and was not continued due to some circumstances, which was planned, however.

Of course, they hadn’t received the report from the university clinic from me here in DO, because dottores are always so offended when others know better, or even more unbearable for the common dottore when the patient knows better.
And then another patient with multiple brain damage.

The pictures now show a visual comparison as to why there was not this first hot lead here at home and therefore could not really point to an ICF syndrome, i.e. with the heterochromatisms of 1qh and 16qh diagnosed years earlier, which I will discuss in detail here in my Human Project One, as yet another indictment of this degenerate so-called healthcare system.

Okay, in picture 1 you can see the orderly arrangement of the chromosome pairs of the Central German University Clinic, in picture 2 you can see the sloppy, reluctance-driven throwing down in the often-experienced Dortmund Dottore style, as it was recently for a long time with the triad with the parathyroid hormone, calcium and phosphate because of my correct suspicion of a pHPT (primary hyperparathyroidism), etc..

Because it was of course psychological for them, the way the inflated report read, as if it had been copied from the literature, as if they had never known anything about ICF syndrome before, which incidentally is considered to be underdiagnosed worldwide, and thus with this special touch to consider the patient to be crazy …