Readings Newsletter
Become a Readings Member to make your shopping experience even easier.
Sign in or sign up for free!
You’re not far away from qualifying for FREE standard shipping within Australia
You’ve qualified for FREE standard shipping within Australia
The cart is loading…

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.
$9.00 standard shipping within Australia
FREE standard shipping within Australia for orders over $100.00
Express & International shipping calculated at checkout
Stock availability can be subject to change without notice. We recommend calling the shop or contacting our online team to check availability of low stock items. Please see our Shopping Online page for more details.
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.