Prenatally diagnosed sacrococcygeal teratoma: A unique expression of trisomy 1q

Cancer Genetics and Cytogenetics

Volumn 117, Issue 1, 2000, Pages 84-86

  Wax, Joseph R ^a   Benn, Peter ^b   Steinfeld, Joy D ^a   Ingardia, Charles J ^a  

^a Dept Obstet Gynecol Hartford H   (United States)

^b UNIVERSITY OF CONNECTICUT SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 1Q; FETUS; FETUS MALFORMATION; HUMAN; KARYOTYPE; PRENATAL DIAGNOSIS; PRENATAL DISORDER; PRIORITY JOURNAL; TERATOMA; TRISOMY;

FEMALE; FETAL DISEASES; HUMANS; KARYOTYPING; PREGNANCY; SACROCOCCYGEAL REGION; TERATOMA; ULTRASONOGRAPHY, PRENATAL;

EID: 0033966255     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00141-7     Document Type: Article

References (5)

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2. Schwartz S., Raffel L.J., Sun C.C.J., Waters E. An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19q and associated with teratoma development. Teratology. 46:1992;399-404.
3. Houri T., Hashimoto N., Ibayashi N., Mori T., Fujimoto M., Ueda S., Abe T., Inazawa J. Chromosome translocation t(1;11)(q12;p15), in an extragonadal immature teratoma. Cancer Genet Cytogenet. 97:1997;79-80.
4. Rooney D.E., Czepulkowski B.H. Prenatal diagnosis and tissue cultures. Rooney D.E., Czepulkowski B.H. Human Cytogenetics. A practical Approach, Vol. 1:1992;53-89 IRC Press, Oxford.
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