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Asking for Self, Female, 28 years old, Lahore
Hi, I wanted to inquire about cousin marriage genetic issues in their children. We had a child with special symptoms. We conceived again. We want to consult hospitals who dela with such issues. Thanking in advance
Please book appointment for discussion in detail!
yes i can guide you in a session. complete family history along with available medical records would be required to discuss the case. Will guide you what possible options do you have to manage this condition.
I can help and guide you properly
You can consider Non-Invasive Prenatal Testing (NIPT) after 10 weeks of pregnancy, as it analyzes cell free fetal DNA. If NIPT indicates a high risk for chromosomal abnormalities, further diagnostic tests such as chorionic villus sampling (CVS) can be performed around 11to14 weeks, or amniocentesis around 16 to 20 weeks for confirmation.
If you already have a child with special needs and no specific genetic disorder has been identified yet, it is advisable to consider genetic screening such as Whole Exome Sequencing (WES) or CMA and karyotyping to investigate potential underlying genetic causes.
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