PK Syndrome is a rare genetic-metabolic disorder-but its impact is far from rare in certain parts of the world. This book offers a interdisciplinary exploration of PK Syndrome with a dedicated focus on Indian and Pakistani populations where the condition is significantly more prevalent due to regional genetic patterns historical marriage traditions and structural healthcare disparities.Combining cutting-edge science with cultural insight the book guides readers through the full landscape of PK Syndrome: its genetic foundations metabolic mechanisms clinical presentations diagnostic challenges long-term outcomes and therapeutic strategies. It also examines the broader contexts in which the disorder unfolds-family structures stigma gender norms migration public health systems and the lived experience of South Asian communities worldwide.From the complexities of variant interpretation to the realities of diagnostic inequity; from precision-medicine opportunities to the cultural dimensions of genetic counselling; from early childhood development to adult life and global policy-this book offers a uniquely integrated view of a condition that crosses borders disciplines and generations.Bremen University Press has published over 5500 specialist books in various languages since 2005.December 2025
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