A rare chromosomal disorder in a newborn: Trisomy 3q
Trisomy 3q is a rare chromosomal disorder that leads to multiple congenital abnormalities. We hereby present a patient with chromosomal karyotype 46, XY, dup (3)(q23-29), which can be classified as pure 3q duplication and has thin sclera and iris dysgenesis, anterior and posterior segment dysgenesi...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hacettepe University Institute of Child Health
2019-04-01
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| Seri Bilgileri: | The Turkish Journal of Pediatrics |
| Konular: | |
| Online Erişim: | https://turkjpediatr.org/article/view/685 |
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