Multicolor chromosomal bar coding characterizes a de novo interstitial deletion (5)(q33.3q35.2) in a child with multiple congenital malformations

We describe a boy with multiple congenital anomalies including a complex heart defect, club feet, adducted thumbs, and facial dysmorphic features. He died at the age of 2 months following cardiac surgery. G-banding analysis identified an abnormal chromosome 5q suspected to be an interstitial deletio...

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Veröffentlicht in:Clinical dysmorphology 2003-04, Vol.12 (2), p.129-131
Hauptverfasser: Schiffer, Christiane, Popp, Susanne, Moshir, Sharareh, Rupprath, Gerhard, Düngfelder, Elke, Hager, Hans-Dieter, Tariverdian, Gholamali, Jauch, Anna
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Sprache:eng
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Zusammenfassung:We describe a boy with multiple congenital anomalies including a complex heart defect, club feet, adducted thumbs, and facial dysmorphic features. He died at the age of 2 months following cardiac surgery. G-banding analysis identified an abnormal chromosome 5q suspected to be an interstitial deletion (5)(q33q35). Breakpoints of the deleted segment were confirmed as del(5)(q33.3q35) by multicolor fluorescence in situ hybridization (FISH) using two sets of combinatorially labeled band specific YAC clones. Findings are discussed in view of previously published cases.
ISSN:0962-8827
DOI:10.1097/00019605-200304000-00011