CameraIcon
CameraIcon
SearchIcon
MyQuestionIcon
MyQuestionIcon
7
You visited us 7 times! Enjoying our articles? Unlock Full Access!
Question

A monosomic (2n1) abnormality in human is

A
Klinefelter's syndrome
No worries! We‘ve got your back. Try BYJU‘S free classes today!
B
Turner's syndrome
Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses
C
Edward's syndrome
No worries! We‘ve got your back. Try BYJU‘S free classes today!
D
Down's syndrome
No worries! We‘ve got your back. Try BYJU‘S free classes today!
Open in App
Solution

The correct option is B Turner's syndrome
  • Klinefelter syndrome is a sex chromosome disorder in boys and men that results from the presence of an extra X chromosome in cells
  • Turner syndrome is due to a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered.
  • Edwards Syndrome (also known as Trisomy 18) is a genetic disorder caused by the presence of all or part of an extra 18th chromosome.
  • Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21
So, the correct answer is 'Turner's syndrome'.

flag
Suggest Corrections
thumbs-up
0
Join BYJU'S Learning Program
similar_icon
Related Videos
thumbnail
lock
Genetic Disorders
BIOLOGY
Watch in App
Join BYJU'S Learning Program
CrossIcon