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Dear Sir/Madam, I am 34 years 11 months of age, Male. Me and My wife have gone for Parental Karyotyping in last September, 2017. My wife test result: Normal female Karyotype. My report result as below: Chromosome analysis revealed male chromosomal pattern with the increase in the length of the satellite on the short arm of chromosome 15 in all metaphase analyzed. However, no specific functions have been associated with the chromosome 15ps+. It is a polymorphic variation seen in the normal population. Last delivery (2 years 7M back) was premature delivery (1 month before) and haa Mass in heart (critical position on LV) rhabdomyoma (?) problem. Does this 46, XY, 15ps+ will affect us in planning a next baby? We are planning for a second bay now. What the precautions to be taken. Confusion to meet gynecologist or Genetic counsellor. Can I know the role of Genetic counsellor? Can any one suggest best genetic counsellor/Gynecologist in Hyderabad?
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As mentioned in report it is variation seen in normal person so nothing to worry and nothing to do. Ideal person to get counselling from is genetic counsellor.
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