There is no satisfactory therapy for many of the disabling genetic disorders such as Wohlfart Kugelberg Welander syndrome. However, it is hoped that advances arising from the accumulating research evidence can contribute to improving treatment of such conditions. Therefore, reviewing the literature for the recent research evidence is recommended to improve the therapeutic services for patients with such disorders. The occurrence of Wohlfart Kugelberg Welander syndrome in Iraq has not been documented before. In addition to providing the historical documentation of this syndrome, particularly the early history of its documentation, this book describes the occurrence of the syndrome in two unrelated Iraqi children. This book also reviews the available research evidence which may contribute to improving its treatment.