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

Résumé

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.


Sujets)
Adulte , Enfant d'âge préscolaire , Délétion de segment de chromosome , Chromosomes humains de la paire 7/génétique , Chromosomes humains de la paire 9/génétique , Analyse cytogénétique , Incapacités de développement/génétique , Études de suivi , Humains , Caryotypage , Mâle , Monosomie/génétique , Phénotype , Translocation génétique/génétique , Trisomie/génétique
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