A specific syndrome due to deletion of the distal long arm of chromosome 1

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Abstract
We have studied 2 patients with de novo deletion 1 (q42.3 → qter): a 5 1/2‐year‐old boy and an unrelated 1 9/12‐year‐old girl. The analysis of the phenotype which is now possible in a total of 23 cases shows that the deletion of the terminal 1q leads to a definable multiple congenital anomalies/mental retardation (MCA/MR) syndrome. The phe‐notype is so characteristic that, as a rule, the clinical data should suggest the correct cytogenetic diagnosis.

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