Genetics for Gynaecologists
A clinically grounded pathway through the genetics most relevant to women's reproductive and antenatal care
12 Hours · 9 Core Modules · 12 CPD · Blended Online · 4 Live Webinars
Clinical genetics is no longer confined to specialist departments — it now sits at the heart of everyday gynaecological practice. From interpreting an expanded carrier screen, through reading a chromosomal microarray report on a fetus with a structural anomaly, to counselling a couple after a positive NIPT, the gynaecologist is increasingly the first point of contact for genetic information.
This 12-hour blended online course is purpose-built for gynaecologists, O&G trainees, midwives, and reproductive health nurses. It provides a clinically grounded, jargon-light but scientifically rigorous pathway through the genetics most relevant to women's reproductive and antenatal care — from chromosomal structure to the nuances of when to order which test and why, ending with a capstone live workshop in genetic counselling.
Programme Goals
- Explain the molecular and chromosomal basis of common conditions encountered in O&G practice in patient-friendly language
- Take, draw, and interpret a three-generation family pedigree and derive recurrence risks
- Recognize syndromic patterns of birth defects on prenatal and neonatal examination and refer appropriately
- Select the right genetic test for the right clinical question using the resolution ladder — karyotype, FISH/QF-PCR, CMA, gene panel, WES/WGS
- Interpret first-trimester combined screening, second-trimester quad, and cfDNA / NIPT reports, including soft markers and special pregnancy scenarios
- Implement expanded carrier screening in the preconception and early antenatal visit, and counsel concordant carrier couples on their reproductive options
- Apply non-directive genetic counselling principles, navigate ethical dilemmas, and integrate with the multidisciplinary genetics team
Target Audience
- Consultant Gynaecologists & Obstetricians — integrate genomics into routine O&G consultations, navigate chromosomal and gene test results confidently, identify when genetic referral is needed, and counsel patients on birth defect recurrence risk
- O&G Trainees & Registrars — build examination-ready genetic knowledge, master inheritance pattern recognition from pedigrees, learn structured test selection, and understand carrier screening in routine antenatal care
- Midwives & Reproductive Health Nurses — explain common genetic tests clearly, support informed consent for antenatal screening, recognise red-flag clinical features for referral, and provide emotionally informed counselling support
- Genetic Counsellor Students (Rotation) — apply GC skills in a gynaecology clinical context, practice communication of serum screening results, navigate obstetric ethical dilemmas, and build competency in prenatal and carrier counselling
Eligibility & Requirements
Academic Eligibility
- MBBS or equivalent medical degree (for clinicians and trainees)
- MD / DNB / DGO / MS in Obstetrics & Gynaecology — for the consultant and trainee tracks
- Registered Midwife or BSc Nursing with active obstetric or reproductive practice
- MSc in Genetic Counselling, Human Genetics, or equivalent (for the GC rotation track)
- Final-year postgraduate students from any of the above streams
Recommended Pre-Course Knowledge
- Working understanding of cell biology and the basic structure of DNA and chromosomes
- Familiarity with the standard antenatal visit schedule and first / second-trimester ultrasound milestones
- Awareness of the PCPNDT Act, 1994 and the MTP Act (with 2021 amendments)
- Comfort reading laboratory reports in English
Technical Requirements
- Laptop or desktop with a stable broadband connection (minimum 5 Mbps recommended)
- Working webcam and microphone — required for live webinars and the capstone role-play workshop
- Modern browser (Chrome, Edge, or Firefox — latest two versions); PDF reader
- Smartphone for the LMS app and on-the-go quiz attempts
Who teaches this course
The programme is led by the Faculty Director, with guest contributions from invited specialist clinicians for specific modules (fetal medicine for Modules 3, 6, and 7; reproductive genetics for Module 8; medical ethics for Module 9). Allelic's teaching style is guidelines-aligned (ACMG, ACOG, RCOG, ESHRE, FIGO, FOGSI) and grounded in Indian and global clinical practice. All cases are de-identified and drawn from real consultations.
Ms. Upasana Mukherjee, MS, CGC
Faculty Director — Board-Certified Genetic Counsellor · 12+ years of clinical experience
Lead faculty across all 9 modules · Live pedigree workshop (Module 2) · Live syndrome recognition session (Module 3) · Live chromosomal Q&A (Module 4) · Screening interpretation workshop (Module 6) · Live carrier counselling seminar (Module 8) · Capstone counselling workshop (Module 9) · Final assessment evaluator. Specialist areas: Reproductive Genetics · Cardiovascular Genetics · Prenatal Genomics · Genetic Counselling Education.
Modules at a glance
9 Core Modules across 12 hours — combining recorded learning, live faculty sessions, and applied assessment.
How you're evaluated
Successful participants receive the Allelic Certificate in Genetics for Gynaecologists, valid for 12 CPD hours, with a verifiable digital QR code. Certificate holders gain 90-day replay access to all course content, the alumni discussion forum, and priority registration for advanced Allelic modules.
Module Quizzes (M1 & M5)
20%10-MCQ quiz after Module 1 (foundations) and Module 5 (gene defects). Best score from unlimited attempts is recorded. Tests recall of foundational and molecular content.
Live Session Participation
20%Attendance and active participation across the four live webinars (Pedigree, Syndrome Recognition, Chromosomal Q&A, Screening Workshop) and the Module 8 carrier seminar. Minimum 3 of 4 webinars + the capstone workshop required. Scored on case-discussion contribution and polling responses.
Decision Flowchart Task (post-M7)
20%Submit a one-page test-selection flowchart for 3 assigned clinical scenarios (e.g., fetus with isolated ventriculomegaly at 22 weeks; couple with two previous unexplained first-trimester losses; primigravida with positive NIPT for T13). Graded on accuracy of test choice, clinical reasoning, and clarity.
Final Integrated Assessment
40%50 single-best-answer MCQs + 4 short-answer clinical vignettes covering all 9 modules. 90-minute timed online exam. Minimum 70% pass mark. Certificate issued on successful completion.
| Component | Description | Weight |
|---|---|---|
| Module Quizzes (M1 & M5) | 10-MCQ quiz after Module 1 (foundations) and Module 5 (gene defects). Best score from unlimited attempts is recorded. Tests recall of foundational and molecular content. | 20% |
| Live Session Participation | Attendance and active participation across the four live webinars (Pedigree, Syndrome Recognition, Chromosomal Q&A, Screening Workshop) and the Module 8 carrier seminar. Minimum 3 of 4 webinars + the capstone workshop required. Scored on case-discussion contribution and polling responses. | 20% |
| Decision Flowchart Task (post-M7) | Submit a one-page test-selection flowchart for 3 assigned clinical scenarios (e.g., fetus with isolated ventriculomegaly at 22 weeks; couple with two previous unexplained first-trimester losses; primigravida with positive NIPT for T13). Graded on accuracy of test choice, clinical reasoning, and clarity. | 20% |
| Final Integrated Assessment | 50 single-best-answer MCQs + 4 short-answer clinical vignettes covering all 9 modules. 90-minute timed online exam. Minimum 70% pass mark. Certificate issued on successful completion. | 40% |
Passing Criteria
- Minimum 70% in the Final Integrated Assessment is required to pass the course
- Module quizzes must be attempted; the best score from unlimited attempts is recorded
- Attendance at minimum 3 of 4 live webinars plus the capstone workshop is required for the live-participation component
- The decision flowchart task must be submitted by the published deadline (one re-submission allowed)
- Participants who narrowly fail (60–69%) may re-take the final assessment once, within 30 days
What you receive
- Allelic 'Quick-Start in Genetics' primer (a 12-page refresher on DNA, chromosomes, inheritance, and mutation)
- Curated glossary of genetic terminology in patient-friendly language
- Sample reports — karyotype, FISH, QF-PCR, CMA, NIPT, gene panel, and trio exome — for orientation
- Pedigree-drawing standard symbols cheat-sheet (PSGC nomenclature)
- Pre-recorded lectures and reading packs — available on the secure LMS with 90-day post-completion replay access
- Structured case packs and downloadable test-selection flowcharts
- De-identified sample reports across karyotype, FISH, QF-PCR, CMA, NIPT, gene panel, and exome
- Pedigree symbols cheat-sheet and genetics terminology glossary
- Six-week schedule with weekly milestones and four faculty-led live sessions
Genetics literacy for every gynaecology consult — practical, rigorous, and built for the clinic.
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