Beschreibung
Non-syndromic agenesis of the corpus callosum is a rare congenital disorder that has not been described or documented in Iraq. In this book, two Iraqi infants with non-syndromic agenesis of the corpus callosum are described. One infant had the isolated type and the second infant had agenesis of the corpus callosum associated with colpocephaly. Both infants had the clinical features of the syndrome resulting from the associated failure of neuronal migration including hypotonia with poor spontaneous movements, and poor head control, and no response to voice. The infant with corpus callosum associated with colpocephaly was treated with a novel therapeutic approach aiming at improving brain functions and accelerating development. She received two medications given by intramuscular injections in five successive therapeutic courses over three months period. Treatment was associated with significant improvement. The second patient didnt receive any specific therapy during three months of observation and he didnt show any obvious improvement despite he didnt have colpocephaly.
Autorenporträt
Aamir Jalal Al Mosawi is advisor in pediatrics and pediatric psychiatry at the Children Teaching Hospital of Baghdad Medical City. He is the Head of Iraq Headquarter of Copernicus Scientists International Panel. He served as a member of the advisory council the International Association of Medical Colleges (IAMC).