|
Author
|
Message
|
upscman
Credits:
2448
My Scrapbook
|
Advanced paternal age is associated with:
|
04.27.04 (4 years ago)
#1
|
|
Advanced paternal age is associated with:
A. New mutations of autosomal dominant disorders
B. Autosomal recessive disorders
C. Cornelia de Lange’s syndrome
D. Down syndrome
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
|
tallpox
Credits:
12032
My Scrapbook
|
|
04.27.04 (4 years ago)
#2
|
|
|
mutns in auto dominant disorders
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
dr_jekyl
Credits:
153
My Scrapbook
|
|
05.01.04 (4 years ago)
#3
|
|
|
tall pox again right.It's mutatations in autosomal dominant!!!
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
sgtkuks
Credits:
4061
My Scrapbook
|
|
08.22.04 (4 years ago)
#4
|
|
|
couldn't it b down's syndrome..........ghai has even mentioned the maternal age specific incedence of down's which actuall increase from some 1;4000 at 30 to 1;25 by 40.........i don't remember exactly
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
Sanya
Credits:
611
My Scrapbook
|
|
08.23.04 (4 years ago)
#5
|
|
Ans: B.Autosomal recessive disorder
1.paternal age is associated with increased AR diseases in children
2. maternal age associate with Down syndrome
I still have some concern about Ans.A
Sanya
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
Akil
Credits:
28144
My Scrapbook
|
|
08.23.04 (4 years ago)
#6
|
|
sgktuks...
its P and not M.........read properly b4 attempting!
its Ok here .....but its NOT OK in PG entrance....
read again the Q.
its paternal and not maternal that is mentioned in the Q!
a definite Googly Q!
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
Akil
Credits:
28144
My Scrapbook
|
|
08.23.04 (4 years ago)
#7
|
|
Advanced paternal age is clearly associated with an increased risk of new mutations.
Examples of new mutant conditions associated with
advanced paternal age include
achondroplasia (a frequent form of dwarfism), neurofibromatosis (NF1),
Marfan syndrome,
Treacher Collins syndrome,
Waardenburg syndrome (a common cause of deafness),
osteogenesis imperfecta (brittle bone disease)
Apert syndrome (a form of acrocephalosyndactyly with an abnormally tall skull, shallow eye sockets, and fusion of fingers and toes).
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
Sanya
Credits:
611
My Scrapbook
|
|
08.23.04 (4 years ago)
#8
|
|
Dear, Akil,
Thanks for your your answer.
Sanya
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
sgtkuks
Credits:
4061
My Scrapbook
|
|
08.25.04 (4 years ago)
#9
|
|
|
ya akil,i know i made a blunder in a hurry............but anyways i'll take care in the future........so u have mentioned the autosomal dominant ones, it means the ans is 'a'.....i trust u
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|
vijs
Credits:
119
My Scrapbook
|
|
12.17.04 (3 years ago)
#10
|
|
|
hi akil where from did u get this list ,its good.
|
|
|
Post Options:
Reply
Add
Forward
Report
New
|
|
Back to top
|
|