0000000001159494

AUTHOR

R. Claramunt

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Prenatally detected double trisomy: Klinefelter and Down syndrome

2006

Double trisomies are a rare occurrence. We report the first case of a Down and Klinefelter's syndrome (48,XXY,+21) in a fetus that was prenatally diagnosed during the 15th week of pregnancy. Even though the nasal bone was present, and the color-Doppler study of the ductus venosus and the nuchal thickness were normal, the maternal serum test results indicated an increased risk of Down syndrome and consequentially a genetic amniocentesis was performed. A 48,XXY,+21 karyotype was observed and the patient decided to terminate the pregnancy. In this case, we did not find the typical ultrasound (US) signs that would have led us to the chromosomopathy; furthermore, we emphasize the advantages of u…

GynecologyPregnancymedicine.medical_specialtyDown syndromeFetusObstetricsObstetrics and GynecologyAneuploidyPrenatal diagnosisBiologymedicine.diseasemedicineKlinefelter syndromeTrisomyGenetics (clinical)Ductus venosusPrenatal Diagnosis
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