Bohring-Opitz syndrome is a rare condition that affects the development of many parts of the body.
Most individuals with Bohring-Opitz syndrome have profound to severe intellectual disability, developmental delay, and seizures. Most affected individuals have a normal head shape and size with no brain abnormalities; however, some have abnormal development of the head. Abnormal development can lead to a small head size and a skull abnormality called trigonocephaly, which gives the forehead a pointed appearance. Structural brain abnormalities can occur with or without head abnormalities. For example, the fluid-filled spaces near the center of the brain (ventricles) may be usually large (ventriculomegaly) or the tissue that connects the left and right halves of the brain (the corpus callosum) can be abnormally thin.
Original Article Source Credits: MedlinePlus , https://medlineplus.gov/
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Link to Original Article: https://medlineplus.gov/genetics/condition/bohring-opitz-syndrome/