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Outcome of a child with Ring chromosome 18 syndrome


Banožić, Ljerka; Šimić Klarić, Andrea; Kolundžić, Zdravko; Tomić Rajić, Marijana; Ćosić, Nada
Outcome of a child with Ring chromosome 18 syndrome // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 94-94 (poster, međunarodna recenzija, sažetak, stručni)


Naslov
Outcome of a child with Ring chromosome 18 syndrome

Autori
Banožić, Ljerka ; Šimić Klarić, Andrea ; Kolundžić, Zdravko ; Tomić Rajić, Marijana ; Ćosić, Nada

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni

Izvornik
Book of abstracts of 12th European Symposium on Congenital Anomalies / - Zagreb : European Surveillance of Congenital Anomalies Association, 2013, 94-94

Skup
12th European Symposium on Congenital Anomalies

Mjesto i datum
Zagreb, Hrvatska, 14.06.2013

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Sy Ring ; outcome ; development

Sažetak
Ring chromosome is structural chromosomal abberation with incidence of 1:50 000 of liveborns. It occurs due to terminal deletion on both chromosomal parts, and then the fusion of rest parts into a ring formation. Until now, there are 70 described cases of Ring cromosome syndrome in literature. The diagnose is often established with delay. He was born from the first pregnancy of non consanguineous parents. Our patient is 11 years old boy with dysmorphic stigmata noticed directly after delivery. He was born in General County Hospital, Požega, Croatia. He was presented with palatoschisis, hypertelorism, lower set ears, short neck, hypospadia, feet malformation and heart murmur. Fallot pentalogy was diagnosed and operated. Further citogenetic analysis established the diagnose of Ring chromosome syndrome: 46xy, r (18), hibridization x, y, numerical adequate. Palatoschisis and feet were operated. He had multiple respiratory infections and was diagnosed as immunodeficiency A. He walked at 6 years of age, but has a psychomotoric retardation and a short stature. He attends a multi-level treatment with speech therapist, psychologist and defectologist. Although patients with Ring chromosome syndrome are mostly diagnosed later in childhood, our patient was diagnosed in early age, in the first months of life, so the treatments of his multiple problems weren't delayed. However, his development is significantly impaired and his congitive functions are much below average.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



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