A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome

Trisomy 13 is a very rare and lethal autosomal chromosomal malformation syndrome. Its incidence is 1/12,000 births. In this paper, we present a new trisomy 13 case associated with unusual and undescribed findings. This patient was the first child of unrelated parents with advanced maternal and pater...

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Veröffentlicht in:	Turkish journal of pediatrics 2008-11, Vol.50 (6), p.595-599
Hauptverfasser:	Balci, Sevim, Güçer, Safak, Orhan, Diclehan, Karagöz, Tevfik
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - pathology Chromosomes, Human, Pair 13 Fatal Outcome Humans Infant, Newborn Male Syndrome Trisomy
Online-Zugang:	Volltext
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