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Ultrasound prenatal diagnosis of congenital primary aphakia: case report
INTRODUCTION: the ultrasound prenatal diagnosis of aphakia is a difficult diagnosis and often requires a genetic study of the karyotype. CASE REPORT: we present a rare case of prenatal bilateral aphakia, confirmed after bird. The patient was observed by ultrasound during the 23rd week of pregnancy....
Tallennettuna:
| Julkaisussa: | J Prenat Med |
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| Päätekijät: | , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
CIC Edizioni Internazionali
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4747566/ https://ncbi.nlm.nih.gov/pubmed/26918094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/jpm/2015.9.1.016 |
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