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Prenatal diagnosis of mosaic trisomy 9
Author(s) -
Zadeh Touran M.,
Peters June,
Sandlin Constance
Publication year - 1987
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1970070110
Subject(s) - trisomy , prenatal diagnosis , fetus , aneuploidy , autopsy , amniotic fluid , obstetrics , pregnancy , medicine , pathology , gynecology , biology , genetics , chromosome , gene
Mosaic trisomy 9 was detected in an amniotic fluid cell culture from a 40‐year‐old woman evaluated because of advanced maternal age. After counselling, parents elected to terminate the pregnancy. On autopsy the fetus was found to have hydrocephalus and a single kidney. The diagnosis of trisomy 9 mosaicism was confirmed in cultured skin fibroblasts. This is the third reported case of trisomy 9 mosaicism diagnosed prenatally.
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