HealthCareMagic is now Ask A Doctor - 24x7 | https://www.askadoctor24x7.com

Get your health question answered instantly from our pool of 18000+ doctors from over 80 specialties
159 Doctors Online

By proceeding, I accept the Terms and Conditions

Dr. Andrew Rynne
MD
Dr. Andrew Rynne

Family Physician

Exp 50 years

HCM Blog Instant Access to Doctors
HCM BlogQuestions Answered
HCM Blog Satisfaction

What Causes Fetal Hypertrophic Cardiomyopathy?

My daughter is 21 weeks pregnant and had an ultrasound the tech wo was doing it said there seemed to be thickening of the heart muscle and it was an indication of Down s syndrome ..she is 23 years old and scared to death does she need to have an amnio
Mon, 6 Apr 2020
Report Abuse
General & Family Physician 's  Response
Hi.

Hypertrophic cardiomyopathy could be reversible in most of the cases but these neonates requires close monitoring and regular follow-up and early intrauterine detection. Its common causes include maternal diabetes, Down syndrome, Noonan syndrome, inborn error of metabolism, and familial single-gene disorder. Consult her gynecologist for possible amniocentesis or chorionic villus sampling to rule out Down's syndrome or other disorders.

Hope I have answered your question. Let me know if I can assist you further.

Regards,
Dr. Mohammed Taher Ali, General & Family Physician
I find this answer helpful

Note: For further follow up on related General & Family Physician Click here.
Disclaimer: These answers are for your information only and not intended to replace your relationship with your treating physician.
This is a short, free answer. For a more detailed, immediate answer, try our premium service [Sample answer]
Share on
 

Related questions you may be interested in


Loading Online Doctors....
What Causes Fetal Hypertrophic Cardiomyopathy?

Hi. Hypertrophic cardiomyopathy could be reversible in most of the cases but these neonates requires close monitoring and regular follow-up and early intrauterine detection. Its common causes include maternal diabetes, Down syndrome, Noonan syndrome, inborn error of metabolism, and familial single-gene disorder. Consult her gynecologist for possible amniocentesis or chorionic villus sampling to rule out Down s syndrome or other disorders. Hope I have answered your question. Let me know if I can assist you further. Regards, Dr. Mohammed Taher Ali, General & Family Physician