Article
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: central nervous involvement in two Italian patients.
European journal of medical genetics - 1 Jan 2000
Terrone Gaetano, D'Amico Alessandra, Imperati Floriana, Carella Massimo, Palumbo Orazio, Gentile Mattia, Canani Roberto Berni, Melis Daniela, Romano Alfonso, Parente Iolanda, Riccitelli Marina, Del Giudice Ennio
Abstract excerpt
The 17q21.31 microdeletion syndrome is a genetic disorder characterized by intellectual disability, facial dysmorphisms and a typical behavioral phenotype. Patients are usually described as friendly and cooperative but they can also show behavioral problems such as hyperactivity, bad humor, tempe...
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