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Indian J Pediatr ; 2008 Sep; 75(9): 956-60
Article in English | IMSEAR | ID: sea-79091

ABSTRACT

Partial trisomy 7p with partial monosomy 9p is a rare disorder with only 3 cases reported. Both these abnormalities i.e., partial trisomy 7p and partial monosomy 9p result in distinct clinical phenotypes. However, patients with combined 7p trisomy/9p monosomy present with a phenotype consistent with trisomy 7p. We present a fourth case of trisomy 7p/monosomy 9p with long term follow-up and document the medical complications associated with this disorder. Long term follow-up of patients with chromosome abnormalities provides a unique opportunity to document the medical history and complications associated with such abnormalities.


Subject(s)
Adult , Child, Preschool , Chromosome Deletion , Chromosomes, Human, Pair 7/genetics , Chromosomes, Human, Pair 9/genetics , Cytogenetic Analysis , Developmental Disabilities/genetics , Follow-Up Studies , Humans , Karyotyping , Male , Monosomy/genetics , Phenotype , Translocation, Genetic/genetics , Trisomy/genetics
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