From first questions to first cries.

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Understand the question before choosing the test

Genetic Counselling

A structured conversation about personal and family history, screening results, diagnostic options, possible results and how each choice could affect pregnancy care.

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The central point
Counselling helps choose and understand a test; it is not itself an invasive procedure.

The discussion separates screening from diagnosis, explains what a test can and cannot answer, and prepares for normal, abnormal, uncertain or incidental results without directing a patient toward one decision.

What the consultation covers

The decisions that need a clear answer.

01

Clarify the referral

Review the scan finding, screening result, previous pregnancy, family history or known condition behind the appointment.

02

Build the relevant history

Record a focused personal, pregnancy and family history rather than ordering a universal panel.

03

Compare options

Explain no further testing, additional screening or diagnostic testing, including timing, scope, limitations and material risks.

04

Plan for results

Discuss how results may be returned, what uncertain findings mean and which specialists or follow-up may be useful.

Practical pathway

What happens in the counselling visit

Bring the records that define the clinical question.

  1. 01

    Review reports

    Bring ultrasound, screening, laboratory and previous pregnancy reports.

  2. 02

    Map the history

    Discuss relatives or pregnancies with relevant diagnosed or suspected conditions.

  3. 03

    Explore choices

    Ask what each option could answer, what it may miss and whether it is time-sensitive.

  4. 04

    Choose the next step

    Take time where clinically possible and arrange the selected test, follow-up or second opinion.

Common questions

Questions about genetic counselling

The aim is informed choice, not pressure toward testing or pregnancy decisions.

Reception can help with appointment details

No. Options may include no further testing, additional screening or a diagnostic procedure depending on the question and patient preference.

Screening estimates chance; diagnostic testing examines a sample for the conditions within the selected laboratory test.

No. Every test has a defined scope, and not every developmental condition is genetic or detectable before birth.

A support person can be helpful. Confirm the clinic’s current companion policy when booking.

No. Maa Clinic does not determine or disclose fetal sex, including through prenatal testing.