Overview

For many decades, the fields of clinical genetics and dysmorphology were largely absent from the Iraqi medical landscape. There were no structured diagnostic pathways, no specialized centers for rare diseases, and minimal local literature to support genetic awareness or dysmorphic diagnosis. As a result, generations of patients with congenital abnormalities and inherited disorders remained undiagnosed or misclassified. However, we have reported an unaccountable number of the first described disorders in Iraq including genetic disorders, syndromes and malformation. This book compiles and analyzes newly documented clinical conditions reported in the literature between 1995 and 2025, providing a focused summary of distinct and previously unclassified disorders, syndromes, and clinical associations. The 15 conditions described in this book include novel syndromes characterized by dysmorphic features, rare neurodevelopmental or endocrine presentations, congenital anomalies, and unclassified genetic disorders. While most were identified through single or limited case observations, they offer unique insights into human variation and disease mechanisms.

Full Product Details

9786208063962

Table of Contents

Reviews

Author Information

Tab Content 6

Countries Available