Utilize este identificador para referenciar este registo:
https://hdl.handle.net/1822/67226
Registo completo
Campo DC | Valor | Idioma |
---|---|---|
dc.contributor.author | Silva, Joana Isabel Igreja da | por |
dc.contributor.author | Ribeiro, Barbara | por |
dc.contributor.author | Cadilhe, Alexandra | por |
dc.contributor.author | Silva, Cristina Isabel Nogueira | por |
dc.date.accessioned | 2020-10-02T08:46:12Z | - |
dc.date.issued | 2019-12-30 | - |
dc.identifier.issn | 1757-790X | - |
dc.identifier.uri | https://hdl.handle.net/1822/67226 | - |
dc.description.abstract | We present a case of a 34-year-old multiparous woman who had been diagnosed with a 14 weeks' gestation showing an abdominal wall bulge possibly representing an omphalocele, containing liver and intestinal loops, at her first-trimester ultrasound scan. At 16 weeks' gestation, an amniocentesis was performed and karyotype analysis revealed a balanced Robertsonian translocation between chromosomes 13 and 14 in a female fetus (45,XX,der(13;14)(q10;q10)). Given this result and ultrasound findings, karyotype and molecular study of the couple were suggested. The results pointed out the absence of maternal contribution to the analysed regions by paternal uniparental disomy for chromosome 14 (isodisomy), which is associated with a severe phenotype. The correlation between ultrasound findings and the genetic study is primordial to guide the diagnostic assessment and to establish the prognosis of the fetal pathology. | por |
dc.description.sponsorship | (undefined) | por |
dc.language.iso | eng | por |
dc.publisher | BMJ Publishing Group | por |
dc.rights | closedAccess | por |
dc.subject | Adult | por |
dc.subject | Amniocentesis | por |
dc.subject | Diagnosis, Differential | por |
dc.subject | Female | por |
dc.subject | Humans | por |
dc.subject | Pregnancy | por |
dc.subject | Pregnancy Trimester, First | por |
dc.subject | Ultrasonography, Prenatal | por |
dc.subject | Uniparental Disomy | por |
dc.subject | Chromosomes, Human, Pair 14 | por |
dc.subject | Prenatal Diagnosis | por |
dc.subject | genetic screening / counselling | por |
dc.subject | ultrasonography | por |
dc.subject | genetic screening | por |
dc.subject | counselling | por |
dc.title | Paternal uniparental disomy for chromosome 14: prenatal management | por |
dc.type | article | por |
dc.peerreviewed | yes | por |
oaire.citationStartPage | e231705(1) | por |
oaire.citationEndPage | e231705(3) | por |
oaire.citationIssue | 12 | por |
oaire.citationVolume | 12 | por |
dc.identifier.doi | 10.1136/bcr-2019-231705 | por |
dc.date.embargo | 10000-01-01 | - |
dc.identifier.pmid | 31892621 | por |
dc.subject.wos | Science & Technology | por |
sdum.journal | BMJ Case Reports | por |
Aparece nas coleções: | ICVS - Artigos em revistas internacionais / Papers in international journals |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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igrejadasilva2019.pdf Acesso restrito! | 146,49 kB | Adobe PDF | Ver/Abrir |