| Complex mosaicism associated with trisomy 9. | |
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MedLine Citation:
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PMID: 8506220 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Fetal karyotypes can be routinely obtained by chorionic villus biopsy, amniocentesis, or fetal blood sampling. Interpretation of results and subsequent counselling can be complicated by pseudomosaicism or mosaicism confined to the placenta or other tissues. We illustrate this by reporting a case of an abnormal fetus with a total of three karyotypically different cell lines (46,XX; 47,XX, +9; and 47,XX, +del(9) (q11) in different tissues (placenta, lung, gonad, and skin). |
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Authors:
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J S Smoleniec; T Davies; P Lunt; P J Berry; D James |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Prenatal diagnosis Volume: 13 ISSN: 0197-3851 ISO Abbreviation: Prenat. Diagn. Publication Date: 1993 Mar |
Date Detail:
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Created Date: 1993-07-02 Completed Date: 1993-07-02 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 8106540 Medline TA: Prenat Diagn Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 211-3 Citation Subset: IM |
Affiliation:
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University Department of Obstetrics, Bristol Maternity Hospital, U.K. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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diagnosis,
genetics Abortion, Therapeutic Adult Biopsy Chromosomes, Human, Pair 9* Female Fetal Diseases / diagnosis, genetics Fetal Growth Retardation / etiology, genetics, ultrasonography Humans Karyotyping Lung / ultrastructure Mosaicism* Oligohydramnios / ultrasonography Ovary / ultrastructure Placenta / ultrastructure Pregnancy Pregnancy Trimester, Third Prenatal Diagnosis Skin / ultrastructure Trisomy* Ultrasonography, Prenatal |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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