In which genetic condition,each cell in the a | vedclass

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(B) Klinefelter's Syndrome is a genetic disorder caused by the presence of an additional copy of the $X$ chromosome in males,resulting in a karyotype

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Klinefelter's Syndrome

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(B) Klinefelter's Syndrome is a genetic disorder caused by the presence of an additional copy of the $X$ chromosome in males,resulting in a karyotype of $47, XXY$.This condition occurs due to the fusion of an abnormal egg $(XX)$ with a normal sperm $(Y)$ or a normal egg $(X)$ with an abnormal sperm $(XY)$.Individuals with this syndrome exhibit masculine development but also show feminine characteristics such as breast development (gynecomastia) and are sterile.

Column $I$	Column $II$
$(A)$ Autosomal trisomy	$(i)$ Turner's Syndrome
$(B)$ Allosomal trisomy	$(ii)$ Mendelian disorder
$(C)$ Allosomal Monosomy	$(iii)$ Klinefelter's Syndrome
$(D)$ Cystic fibrosis	$(iv)$ Down's Syndrome

In which genetic condition,each cell in the affected person has three sex chromosomes $XXY$?

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Match the Column $I$ with Column $II$:
Column $I$ Column $II$
$(A)$ Autosomal trisomy $(i)$ Turner's Syndrome
$(B)$ Allosomal trisomy $(ii)$ Mendelian disorder
$(C)$ Allosomal Monosomy $(iii)$ Klinefelter's Syndrome
$(D)$ Cystic fibrosis $(iv)$ Down's Syndrome

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