Ultrasound prenatal diagnosis of a de novo 14q distal duplication associated with foetal anomalies: a case report
| Autor: | Giana Izzo, Luisa Ronzoni, Maria Angela Rustico, Mariano Lanna, Anna Garofalo, Valentina Toto |
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| Rok vydání: | 2020 |
| Předmět: | |
| Zdroj: | Case Reports in Perinatal Medicine. 9 |
| ISSN: | 2192-8959 2192-8932 |
| DOI: | 10.1515/crpm-2020-0032 |
| Popis: | Objectives Partial trisomy 14q is a rare chromosomal abnormality with an extremely variable phenotype ranging from mild to severe forms of malformation. Most of the cases described in literature are postnatal clinical findings although few prenatal cases have been reported. Case presentation A 33-year-old woman at 21+6 weeks’ gestation was referred to our hospital for a detailed foetal ultrasound with suspected partial agenesis of corpus callosum and ureterocele. On examination, we found a short corpus callosum and ureterocele with a duplicated right renal collecting system. Moreover, there was an intrarotation of left foot with a prominent part departing from the ankle, both thighs appeared thicker, a thickening of the nuchal fold, a mild hypertelorism and a thick heterogeneous placenta. The patient underwent magnetic resonance imaging (MRI), which confirmed the foetal anomalies. The couple opted for a termination of pregnancy. Chromosome analysis and molecular karyotyping of amniocytes revealed a de novo rearrangement of chromosome 14 with an interstitial gain 14q31.1–14q32.22 and a terminal deletion 14q32.33. Conclusions The majority of partial trisomy 14q reporter are postnatal diagnoses. Improvement in the quality of foetal imaging and molecular techniques have made possible to identify many genetic syndromes prenatally. In our opinion, anomalies of the brain, urinary system and limbs may be the core findings of trisomy 14q. To our knowledge, no such case has ever been described previously. |
| Databáze: | OpenAIRE |
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