Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome

Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome is characterized by multiple fractures in the prenatal period, microcephaly and bilateral cataracts. It has been described in three infants all of whom died in utero or a few hours after birth. The mode of inheritance appears to be autosomal recessive.

Also known as: osteogenesis imperfecta congenita, microcephaly, and cataracts

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome itself.