Explain :
#Turner's Syndrome.
#Klinefilter's Syndrome.
#Down's Syndrome.
#Alkaptonuria.
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1. Turner syndrome is a chromosomal condition dat alters development in females. Women wid this condition tend to be shorter than average and r usually unable to conceive a child because of an absence of ovarian function.
2. Klinefelter syndrome is a genetic condition that results when a boy is born with an extra copy of the X chromosome. Klinefelter syndrome is a common genetic condition affecting males.
3. Down syndromes is a condition in which extra genetic material causes delay in the way a child develops, both mentally and physically.
4. Alkaptonuria is an inherited disorder. People with alkaptonuria can not properly metabolize phenylalanine and tyrosine.
2. Klinefelter syndrome is a genetic condition that results when a boy is born with an extra copy of the X chromosome. Klinefelter syndrome is a common genetic condition affecting males.
3. Down syndromes is a condition in which extra genetic material causes delay in the way a child develops, both mentally and physically.
4. Alkaptonuria is an inherited disorder. People with alkaptonuria can not properly metabolize phenylalanine and tyrosine.
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turners
syndrome-a genetic defect in which affected women have only one X chromosome,
causing developmental abnormalities and infertility
klinefilter's syndrome-a syndrome affecting males in which the cells have an extra X chromosome (in addition to the normal XY), characterized by a tall thin physique, small infertile testes, and enlarged breasts.
Down syndrome- a congenital disorder arising from a chromosome defect, causing intellectual impairment and physical abnormalities including short stature and a broad facial profile. It arises from a defect involving chromosome 21, usually an extra copy
Alkaptonuria-(black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic disorder in which the body cannot process the amino acidsphenylalaine and tyrosine, which occur in protein. It is caused by a mutation in the HGD gene for the enzyme homogentisate 1,2-dioxygenase
klinefilter's syndrome-a syndrome affecting males in which the cells have an extra X chromosome (in addition to the normal XY), characterized by a tall thin physique, small infertile testes, and enlarged breasts.
Down syndrome- a congenital disorder arising from a chromosome defect, causing intellectual impairment and physical abnormalities including short stature and a broad facial profile. It arises from a defect involving chromosome 21, usually an extra copy
Alkaptonuria-(black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic disorder in which the body cannot process the amino acidsphenylalaine and tyrosine, which occur in protein. It is caused by a mutation in the HGD gene for the enzyme homogentisate 1,2-dioxygenase
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