Holoprosencephaly is a complex congenital disorder that manifests itself in a variety of ways and develops from a number of causes. This work offers a detailed study of the various facets of this disorder, covering the many anatomic variations and possible conditions that may occur. The history, etiology, epidemioloy, anatomy and neuropathology, normal and abnormal embryology, and clinical diagnosis and related disorders are thoroughly discussed. The cases of thirty five infants affected with this disease are described. Offering the most extensive and profusely illustrated description of this disorder, this text is a must for health care professionals who treat and care for these infants.
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