Syndromes with ADHD

group of genetic connective tissue disorders

T cell deficiency disease that is the result of a large deletion of chromosome 22, which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production

congenital disorder of nervous system

autosomal recessive disease that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life

multiple congenital anomaly caused by deletion on chromosome 11, often featuring intellectual disabilities, dysmorphic features, delayed development and heart defects.

rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea

disease