Duplication of 9q12-q33: A case report and implications for the dup(9q) syndrome

We report on a boy with a direct tandem duplication of 9(q12‐q33) and dolichocephaly, beaked nose with prominent philtrum, deepset eyes, receding small chin, failure to thrive, developmental delay, simian creases, long fingers, stiff joints, and hypoplastic scrotum. This patient is compared to the 5...

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Veröffentlicht in:American journal of medical genetics 1993-02, Vol.45 (4), p.456-459
Hauptverfasser: Stalker, Heather J., Aymé, Ségolène, Delneste, Daniele, Scarpelli, Hélène, Vekemans, Michel, Der Kaloustian, Vazken M.
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Sprache:eng
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Zusammenfassung:We report on a boy with a direct tandem duplication of 9(q12‐q33) and dolichocephaly, beaked nose with prominent philtrum, deepset eyes, receding small chin, failure to thrive, developmental delay, simian creases, long fingers, stiff joints, and hypoplastic scrotum. This patient is compared to the 5 other reported cases with pure partial dup(9q), and the “trisomy 9q syndrome” described by Turleau et al. [1975]. © 1993 Wiley‐Liss, Inc.
ISSN:0148-7299
1096-8628
DOI:10.1002/ajmg.1320450412