10q-Syndrome (10q Deletion Syndrome) 1221

General: Chromosome 10q deletion syndrome.

Ocular: Microphthalmia.

Clinical: Intrauterine growth retardation; microcephaly; truncus arteriosus type I; respiratory distress; craniofacial dysmorphism.

Glanz AS, et al. Lenz microphthalmia: a malformation syndrome with variable expression of multiple congenital anomalies. Can J Ophthalmol 1983; 18:41-44.

Lewandowski RC, et al. Partial deletion 10q. Hum Genet 1978; 42:339-343.

Taysi K, et al. Terminal deletion of the long arm of chromosome 10:q26 to qter. Case report and review of literature. Ann Genet 1982; 25:141-144.