American Journal of Medical Genetics 42:665-666 (1992)

Brief Clinical Report del(18p) Syndrome With Complex Tetralogy of Fallot in an Infant With 45,X,t(Y;18)(q12;ql1.2) S. El Kalla, A.R. Mathews, and N.S. Menon Department of Pediatrics and Genetics, A1 Wasl Maternity and Pediatric Hospital, Dubai, United Arab Emirates also had a depressed nasal bridge with a short nose, a prominent elongated philtrum with downturned corners of the mouth, medial epicanthal folds, apparently low-set ears with prominent auricles, and brachydactyly and clinodactyly of the 5th finger on both hands, with proximally displaced thumbs and pectus carinatum (Figs. 1 and 2). At 16 months his weight was

del(18p) syndrome with complex tetralogy of Fallot in an infant with 45,X,t(Y;18)(q12;q11.2).

We report on an infant with multiple congenital anomalies, tetralogy of Fallot, and Karyotype 45,X,t(Y;18)(q12;11.2). The infant's anomalies are consi...
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