OSCE in Fetal Medicine and Genetics for Fetal Medicine Fellowship Exam Candidates | Organ-wise OSCE Stations with Image-based Scenarios on Prenatal Diagnosis, Ultrasound and Genetic Counseling: 1

OSCE in Fetal Medicine and Genetics is a first-edition, exam-format book built entirely around Objective Structured Clinical Examination (OSCE) stations for fetal medicine and genetics. It is endorsed by FOGSI and is described as the first book of its kind in this sub-specialty. The book is organised so that each chapter takes one organ system or one subject area of fetal medicine and genetics and presents 15 to 20 OSCE stations on it. Most stations are built on images and illustrations, so the reader practises interpreting the same ultrasound pictures, scan findings and pedigrees that appear in the real fellowship examination and in clinic. Across 24 chapters the stations move through prenatal screening and diagnosis, first and second trimester ultrasound, structural fetal anomalies by system, genetic testing and its interpretation, and counselling of parents. The stated aim is to give students, fellows and practising fetal medicine specialists a more objective, scenario-based way to work through problems they meet in practice, and to build confidence in counselling parents and managing affected pregnancies. Each station provides a structured model answer. Who This Book Is For: Candidates for Fellowship examinations in Fetal Medicine: targeted practice in the exact OSCE format, with image-based stations and model answers for prenatal diagnosis, ultrasound and genetics. Practising fetal medicine specialists, perinatologists and maternal-fetal medicine consultants: a structured refresher on scan interpretation, genetic-test reporting and parent counselling for day-to-day clinic work. Why This Book Helps: Format-specific practice: stations mirror the fellowship OSCE, so preparation is spent on answering in the way the exam scores. Image interpretation drill: most stations turn on ultrasound images and pedigrees, training pattern recognition for fetal anomalies and screening findings. Counselling structure: station answers give a repeatable framework for explaining results, risks and options to parents under time pressure. Sub-specialty coverage in one place: organ-by-organ fetal anomalies plus genetics and screening are gathered into a single scenario-based resource. Key Features: 24 chapters, each covering one organ or subject area of fetal medicine and genetics. 15 to 20 OSCE stations per topic, each with a structured model answer. Image-based stations using ultrasound pictures, scan findings and pedigrees. Coverage of first and second trimester screening, prenatal diagnosis, fetal anomalies and genetic counselling. Endorsed by FOGSI; first dedicated OSCE resource in fetal medicine and genetics.

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