Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection

An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations i...

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Veröffentlicht in:	Obstetrics and gynecology (New York. 1953) 1987-09, Vol.70 (3), p.449-452
Hauptverfasser:	Benn, Peter A., Hsu, Lillian Y. F., Verma, Ram S., Alonso, Lita M., Reich, Elsa, Wishnick, Marcia
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Chromosome Banding - methods Chromosome Deletion Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 5 Cri-du-Chat Syndrome - diagnosis Female Fetal Diseases - diagnosis Gynecology. Andrology. Obstetrics Humans Karyotyping Management. Prenatal diagnosis Medical sciences Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis - methods Translocation, Genetic
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Zusammenfassung:	An unbalanced translocation, 46,XX,der(5)t(5;11) (p15;q25)mat was ascertained by prenatal diagnosis. The mother previously had a liveborn child with cri du chat syndrome. The subtlety of the chromosome rearrangement in this case illustrates the need for the most detailed cytogenetic investigations in cri du chat cases when deletion or translocation are not immediately obvious. (Obstet Gynecol 70:449, 1987)
ISSN:	0029-7844 1873-233X