Holoprosencephaly is a congenital disorder characterized by the incomplete separation of the forebrain during early embryonic development, leading to various degrees of malformation in the brain and facial structures. This condition can result in significant neurological deficits and a range of physical anomalies, impacting the overall development of affected individuals. Holoprosencephaly is often associated with other congenital disorders and can arise due to genetic factors, environmental influences, or both.
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