10q-Syndrome (10q Deletion Syndrome) 111f56b 111f56b 111f56b 111f56b
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-l44.
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