Cephalopolysyndactyly Orofacial Clefts Disorders of Sexual Development Renal Anomaly with Hirschsprung’s Disease an unexpected Spectrum of Anomalies under Chromosome Partial Monosomy 7 with a deletion in the p21.3 segment: Clinical Image - Abstract
Chromosome microdeletion is a hereditary disease with complex clinical manifestations due to the deletion of small chromosome segments [1]. Chromosome 7, Partial Monosomy 7p is a rare chromosomal disorder characterized by deletion (monosomy) of a portion of the short arm (p) of chromosome 7 (7p) [2]. Associated symptoms and findings may be variable and may depend on the specific size and location of the deleted segment of 7p [2].