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Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and
N Schmidt1, D C Van Dyke, K Keppler-Noreuil
1Department of Pediatrics, Children's Hospital of Iowa, Iowa, USA.
Developmental Medicine and Child Neurology
|February 28, 2001
Abstract:
A male child with multiple congenital anomalies and developmental delay is described. Cytogenetic evaluation showed that the patient was partially monosomic for the short arm of chromosome 18 and partially trisomic for the short arm of chromosome 16: a combination of chromosomal syndromes not previously described.