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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
The phenotypic spectrum of trisomy 2: report of two new cases
Ercan Mihci1, Gopalrao V N Velagaleti, Regina Ensenauer
1Department of Medical Genetics, Mayo College of Medicine, Rochester, Minnesota 55905, USA.
Clinical Dysmorphology
|May 29, 2009
Abstract:
We describe two cases of trisomy 2. The first case is a child with mosaic trisomy 2 who presented with mental retardation, multiple congenital anomalies, and dysmorphic findings similar to Pallister-Killian syndrome. The second case was an acardiac and acranial fetus with complete trisomy 2. We review the phenotypic spectrum associated with trisomy 2.
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