A unique case of recurrent fetal cystic hygroma: first fetus with an inherited heteromorphism of chromosome 1 (1qh+) and the second fetus with 69XXX triploidy

The authors report a unique recurrent septated cystic hygroma (CH), on two successive pregnancies, at five years interval. The chromosome analysis of the first fetus showed an increase in length of heterochromatin on the long arm of chromosome 1 – 1qh+, a chromosomal polymorphism inherited from moth...

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Detalles Bibliográficos
Autores principales: Tica, Oana Sorina, Gug, Cristina, Tica, Andrei Adrian, Busuioc, Cristina Jana, Amiri, Shahram, Tica, Irina, Brăiloiu, George Bică, Tica, Vlad Iustin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112748/
https://www.ncbi.nlm.nih.gov/pubmed/33817737
http://dx.doi.org/10.47162/RJME.61.3.34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112748/
https://www.ncbi.nlm.nih.gov/pubmed/33817737
http://dx.doi.org/10.47162/RJME.61.3.34

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