A further case of monosomy 10qter

Abstract
A child with a terminal deletion of chromosome 10 (q26) is described. A comparison of the phenotypic and cytogenetic features is made in the 5 reported cases of monosomy 10qter. No phenotypic features are found sufficiently characteristic to delineate a syndrome. Enzymatic activities for PGAMA [phosphoglycerate mutase] and GOT1 [glutamate oxaloacetate transaminase] were normal.