question-icon

What Does My Ultrasound Scan Test Report Indicate?

default
Posted on Tue, 12 Jul 2016
Question: Hello doctor,
This is XXXX from Vellore. I would like to ask you regarding my wife's pregnancy. This is our second baby and she is now 33 weeks and everything was normal until the recent scan which showed the following,
1. Long bones are short by 3-4 weeks. Femur,Humerus,Fibula,Tibia,Radial,Ulna.
2. Left Femur is bent.
HC, BPD, AC all are normal. Femur to Foot length ratio is 0.77
TC/AC ratio normal. Late onset Skeletal Dysplasia with no signs of lethality.
Planned for normal vaginal delivery.
They have ruled out Down's but we are afraid of the physical appearance of the baby. And moreover we do not have a family history of any genetic malformations. I am 5'9 and my wife is 5'4. Our first child is a girl baby and is one and a half year old healthy child but she too was an IUGR baby with birth weight of 2.24 kg.
I have attached the scan reports along with this.
We would like to know if the baby will be normal physically and what can be done about the femur bent? How to increase bone growth and fetal weight since there is some more time left for the delivery.?





Hello Doctor,
Thank you for your reply. I would like to ask you 2 things:
1. What is a Level II scan and can it be taken now at 33+ weeks?
2. Tomorrow is my sppointment with the genetic specialist. What all shoud i discuss with him?

regards.
doctor
Answered by Dr. Manisha Jain (39 minutes later)
Brief Answer:
Serious issue

Detailed Answer:
Hello sir, thanks for trusting health care magic.
It us indeed a serious situation and cannot be managed by diet or medicine.
I would like you to discuss the issue with a genetic specialist and get a level 2 scan from a fetal radiologist.
Must take it seriously and at the earliest and opt for normal delivery as much as possible.
All the best.
Regards
Dr Manisha




Brief Answer:
Get a level 2 scan

Detailed Answer:
Level 2 scan is done at 16-18 weeks usually as it is to see gross problems in formation of various organs in the baby.
Another level 2 scan is indicated at 32-34 weeks which is done only in high risk cases with history or examination is suggesting some serious issue with the growth and development of the baby.
Get it done and then we can discuss the matter.
Genetic counselling is very important in your case so as to see if anything in both of you is present which has led to such findings in the baby.
Also ask him precautions in future and if anything is needed prior to planning next pregnancy and any blood tests needed to see the extent and cause of problems.
Best answer will be given by fetal karyotyping most likely but he will be the best guide to management now.
All the best dear.
Note: For further follow up on related General & Family Physician Click here.

Above answer was peer-reviewed by : Dr. Chakravarthy Mazumdar
doctor
Answered by
Dr.
Dr. Manisha Jain

OBGYN

Practicing since :2007

Answered : 5136 Questions

premium_optimized

The User accepted the expert's answer

Share on

Get personalised answers from verified doctor in minutes across 80+ specialties

159 Doctors Online

By proceeding, I accept the Terms and Conditions

HCM Blog Instant Access to Doctors
HCM Blog Questions Answered
HCM Blog Satisfaction
What Does My Ultrasound Scan Test Report Indicate?

Brief Answer: Serious issue Detailed Answer: Hello sir, thanks for trusting health care magic. It us indeed a serious situation and cannot be managed by diet or medicine. I would like you to discuss the issue with a genetic specialist and get a level 2 scan from a fetal radiologist. Must take it seriously and at the earliest and opt for normal delivery as much as possible. All the best. Regards Dr Manisha Brief Answer: Get a level 2 scan Detailed Answer: Level 2 scan is done at 16-18 weeks usually as it is to see gross problems in formation of various organs in the baby. Another level 2 scan is indicated at 32-34 weeks which is done only in high risk cases with history or examination is suggesting some serious issue with the growth and development of the baby. Get it done and then we can discuss the matter. Genetic counselling is very important in your case so as to see if anything in both of you is present which has led to such findings in the baby. Also ask him precautions in future and if anything is needed prior to planning next pregnancy and any blood tests needed to see the extent and cause of problems. Best answer will be given by fetal karyotyping most likely but he will be the best guide to management now. All the best dear.