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Journal of the Korean Pediatric Society ; : 683-686, 2001.
Article in Korean | WPRIM | ID: wpr-163495

ABSTRACT

A ring 18 chromosome(18r) karyotype is a rare disorder characterized by short stature, obesity, microcephaly, mental retardation, micropenis, cryptorchidism, hypertelorism, epicanthal folds, micrognathia, and small hands with short tapering fingers. A 22-month-old girl was referred to our department of pediatrics because of ptosis and delayed development. Karyotype revealed ring 18 and dicentric ring 18 chromosome(46,XX,r(18)[45]/45,XX,-18[7]/46,XX,dic r(18)[3]). Fluorescent in situ hybridization with 18 centromeric probe showed 18 ring chromosome with 1 signal and 18 dicentric ring chromosome with 2 signals. We report a case of a ring 18 chromosome diagnosed by karyotype and fluorescent in situ hybridization.


Subject(s)
Female , Humans , Infant , Male , Cryptorchidism , Fingers , Hand , Hypertelorism , In Situ Hybridization, Fluorescence , Intellectual Disability , Karyotype , Microcephaly , Obesity , Pediatrics , Ring Chromosomes
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