Dr Oukacha Nadia - Obstetrics specialist in Casablanca

Amniocentesis

This is an amniotic fluid sampling (puncture) technique used for antenatal diagnosis.

Amniocentesis is an invasive medical procedure in which a needle is used to extract around 20 ml of fluid from the amniotic cavity in which the fetus remains throughout pregnancy.

It can be performed from 14 weeks of amenorrhea to the end of the pregnancy.

Amniocentesis is used to :

A fetal karyotype with the search for chromosomal abnormalities such as trisomy 21, trisomy 13, trisomy 18, monosomy X, 0

Testing for potentially serious fetal infections, such as toxoplasmosis, cytomegalovirus or rubella, which can cause fetal malformations or abnormal fetal development.

Research into certain potentially serious hereditary genetic diseases

The determination of alpha-fetoprotein in amniotic fluid, a marker for certain neurological anomalies of fetal development such as spina bifida.

Amniocentesis is proposed when, during pregnancy, there is a risk that the fetus may carry a potentially serious disease.

These situations arise when :

  • First-trimester ultrasound reveals an anomaly suggestive of chromosomal malformation (nuchal translucency ≥ 3 mm)
  • Screening for trisomy 21 is positive, showing a high integrated risk of chromosomal anomaly. This screening integrates the risk linked to maternal age, the risk linked to nuchal translucency thickness measured at first-trimester ultrasound, and the risk linked to the level of serum markers measured at the same time in maternal blood.
  • Maternal age > 38 years at the time of amniocentesis if ultrasound and serum screening have not been performed on time (the age threshold of over 38 years is arbitrary and corresponds to a risk of chromosomal abnormality greater than or equal to 1/250).
  • Ultrasound signs suggestive of chromosomal abnormality during 2nd or 3rd trimester ultrasound (cardiac malformation; renal malformation; certain cases of intrauterine growth retardation, etc.).
  • History of a child with a chromosomal abnormality
  • One of the parents has a chromosomal abnormality.

Care philosophy

A holistic approach to women's health

Dr Nadia Oukacha puts her expertise in gynecology, obstetrics and fertility at the service of every woman, combining listening, prevention and cutting-edge technology.

Active listening and caring

Each consultation begins with an in-depth discussion to understand your needs and establish a climate of trust.

Comprehensive, personalized approach

A complete check-up, nutritional advice and psychological follow-up are adapted to your age and life situation.

Focus on prevention

Regular smear tests, screening and check-ups aim to anticipate risks and preserve your health over the long term.

Frequently asked questions (FAQ)

Here you'll find answers to the most frequently asked questions about consultations, specialties, booking appointments and how the practice works.

How do I make an appointment with Dr Oukacha?

You can book your consultation directly online via our website or by calling the practice on +212 606 12 12 13. A contact form is also available on the site.

What are Dr Nadia Oukacha's specialties?

Dr Oukacha specializes in :

  • Gynecology (consultations, pap smears, colposcopy, ultrasounds)

  • Obstetrics (pregnancy monitoring, ultrasound, amniocentesis)

  • Intimate and breast surgery

  • Fertility and medically assisted reproduction (MAP)

What examinations are carried out at the clinic?

The practice is equipped for :

  • Gynecological and obstetrical ultrasounds

  • Cervico-vaginal smear

  • Colposcopy

  • Fertility assessment

What are the opening hours?

  • Monday to Friday: 9:00 am - 5:00 pm

  • Saturday: 9:00 am - 1:00 pm

  • Sundays and public holidays: closed

Where is the office located?

The office is located in Casablanca, at 125 BD Brahim Roudani, 1st floor, Appt 11. An interactive map is available on the Contact page.

Book your consultation

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