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rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
1993-7-2
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|
pubmed:abstractText |
We report a case of chromosomal mosaicism for monosomy 21 revealed in amniotic fluid cell culture. Ultrasound examination at 19 weeks' gestation showed in utero growth retardation and a complex cardiac malformation. A repeated amniocentesis confirmed the presence of monosomy 21 mosaicism. In view of the sonographically detected fetal abnormalities, termination of pregnancy was elected.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:month |
Mar
|
|
pubmed:issn |
0197-3851
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
13
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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|
pubmed:pagination |
163-9
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|
pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:8506217-Abnormalities, Multiple,
pubmed-meshheading:8506217-Abortion, Therapeutic,
pubmed-meshheading:8506217-Adult,
pubmed-meshheading:8506217-Amniocentesis,
pubmed-meshheading:8506217-Chromosomes, Human, Pair 21,
pubmed-meshheading:8506217-Echocardiography,
pubmed-meshheading:8506217-Facial Bones,
pubmed-meshheading:8506217-Female,
pubmed-meshheading:8506217-Fetal Diseases,
pubmed-meshheading:8506217-Fetal Growth Retardation,
pubmed-meshheading:8506217-Fingers,
pubmed-meshheading:8506217-Heart Defects, Congenital,
pubmed-meshheading:8506217-Humans,
pubmed-meshheading:8506217-Monosomy,
pubmed-meshheading:8506217-Mosaicism,
pubmed-meshheading:8506217-Pregnancy,
pubmed-meshheading:8506217-Pregnancy Trimester, Second,
pubmed-meshheading:8506217-Prenatal Diagnosis,
pubmed-meshheading:8506217-Ultrasonography, Prenatal
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|
pubmed:year |
1993
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|
pubmed:articleTitle |
Prenatal detection of monosomy 21 mosaicism.
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|
pubmed:affiliation |
Department of Pathology, Mount Sinai School of Medicine, New York, NY 10029.
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pubmed:publicationType |
Journal Article,
Review
|
