We report on a 14-month-old girl with bifid nasal tip and tetralogy of Fallot. Several similar patients have been described with CNS or eye abnormalities. Chromosome analysis with FISH, using Oncor DiGeorge probes, confirmed a submicroscopic deletion of 22q11. Many patients with Shprintzen (velo-car
✦ LIBER ✦
Left hemitruncus associated with tetralogy of Fallot: A case report
✍ Scribed by Mustafa Soylu; Ahmet Duran Demir; Hakan Tikiz; Halil Kisacik; Şule Korkmaz
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 97 KB
- Volume
- 51
- Category
- Article
- ISSN
- 1522-1946
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## Abstract A newborn male had an interstitial deletion of 16q21–q22.1 accompanying tetralogy of Fallot associated with pulmonary atresia and major aortopulmonary collateral arteries (MAPCA), dysmorphic craniofacial features, failure to thrive, and severe psychomotor developmental delay. When the d