MICRO syndrome

Warburg Micro syndrome (WARBM), also known as Micro syndrome, is a rare autosomal recessive genetic disorder characterized by microcephaly, microcornea, congenital cataract, intellectual or developmental disability, optic atrophy, and hypogenitalism. Genetics The rare cases that have been examined are often within families, or the people that have cases of Warburg Micro syndrome have a mutation in their genes.It can be associated with RAB3GAP. Diagnosis Warburg Micro syndrome can be identified in people several ways, one of the most common is ocular problems or other physical traits that don't appear natural. [Source: Wikipedia ]