“THE DISGENEZIES OF MULLER CANALS AT 4-5 MONTHS,THE EMBRYONARY AGE IN THE SUPERIOR ENERGETICAL PART,REPAIRED INCOMPLETELY AT 6 – 8 EMBRYONARY MONTHS LEADS THE ADULT PACIENT, 28 YEARS OLD ,TO A PRIMARY INFERTILITY VERY DIFFCULT TO BE TREATED”.CLINICAL CYTO-GENETIC CAS:TURNER SYNDROME Cs. 45XO MOSAICAL AT 15%, WITH IS Cs.17 DEFECTIVE-LESIONAL CONSTITUTED,BY NEAR HIDDEN. THE ENERGETICAL”IN VIVO” INVESTIGATIONS,( and in concomitance “in retro” age , embryologycal) .”

 

 CristianCalcan,Mariana Calcan.,“NEW ENDOCRINOLOGY”Research Center, Buzau ,Romania .

 

Clinical cas :Turner Syndrome Chromosomes :Cs.45 XO ,mosaical at 15%, with is Cs. 17 defective energetical and lesional constituted and primordial lesional-functional Cs.X1,with a primary infertility at female-pacient of 28 years old (hidden-by near inexpressible) ,with a congenitals malformations of uterus with “difidus”and bicornous aspect, with hypo-ovarism and a small uterus in embryonary life from 3 to 5 months, having a repair by imperfect embryonary joining in the 8th or 9th month..it keeps on having an aspect of fibrosis,uterus-ovarian,obtained immediately after birth,maintained later as an adult

 

 Today she presents the periodic amenorrhoea and a formal permanent  hypo-ovarism,with fibrosis the right ovary,  with negative consequences at the uterus( micro-ansilar, medio-cupolar rugous area)with psycho-socio-familiar anxieties, without secondary sexual negativism and the secondary disgenesis(and is the urinare bladder,with medio fibrosis-strap,and functional dysuria),slight anatomical modifications.

 

 The patient is normal apparently, but she is infertile,in spite of the treatment made in hopital(with intermittently)in the latest 5 years.At the cytogenetics,the cytological, chromozomials and examination she presents the following aspects:

 

  Aster-spindles are imperfect morphologically and energetical functionally (and the signals lesionals at  Cs.X1(leading) and Cs.X2,the  “p” 1 ,1.2 and “q” 1.2 ,2 ,2.2 legs) (1) ,

-          Cellular division presents frequent apparition of cells without Barr corpuscles (2),..

-          -Cyto-genetic in proportion 15% mosaical Cs.45XO,with chromosomes X1,X2-energetical lesional disfunctions,cells:hypercromatinien nucleus,with a bigger cytoplasmas (3) associated to normal cells 80%.

 

The etiology of the troubles of the primitive functions at the age of 3-4 months of the embryo corpus is:Muller Canals are energetical distorting,with troubles of the urinary bladder’s constitution and of uterus-ovary, and presented at the urinary bladder after birth,troubles that are present also at the moment of the adult patient’s consultation ...in embryonary version .

Study of endocrine embryological energetical  medicine at the”New Endocrinology” Research Center .

 

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Text : 353 mots  dr.Calcan Cristian

 

For  23 Joint Meeting of the British Endocrine Societies 22-24 March 2004,The Brighton Centre U.K.

Reproduction category.

Cristian Calcan,New endocrinology, research center,Buzau,Romania.Adres:Dr.CristianS.Calcan membre BES,26,CRISAN ,5100,BUZAU,ROMANIA

website : http://newendocrinology.buzau.ro ;E-mail:calcan@buzau.ro