PMID: 11913572Mar 27, 2002Paper

Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p

Journal of Child Neurology
Gideon EshelJoseph Barr

Abstract

We report a child with craniosynostosis, partial absence of the corpus callosum, developmental delay, precocious puberty, and deletion of chromosome 9(p12p13,3). A review of the literature did not reveal any previous combination of the same kind. Craniosynostosis and partial absence of the corpus callosum, separately or in conjunction, may be part of the spectrum of malformations in the chromosome 9p deletion syndrome, and its presence, in combination with other known features, should prompt a search for this particular deletion as part of the differential diagnosis.

References

Nov 1, 1988·Journal of Medical Genetics·J L HuretJ Lejeune

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Citations

Jan 6, 2016·American Journal of Medical Genetics. Part a·Megan Crone, Mary Ann Thomas
Feb 9, 2010·Anales de pediatría : publicación oficial de la Asociación Española de Pediatría (A.E.P.)·F J Climent AlcaláR Gracia Bouthelier
Jun 18, 2009·American Journal of Medical Genetics. Part a·Ariana KariminejadMohammad Hasan Kariminejad
Aug 5, 2010·American Journal of Medical Genetics. Part a·Mary C O'DriscollWilliam B Dobyns
Aug 14, 2012·American Journal of Medical Genetics. Part a·Anna-Kaisa NiemiMelanie A Manning
May 27, 2016·Journal of Korean Neurosurgical Society·Su-Kyeong HwangSung Kyoo Hwang
Jan 7, 2006·Health Education & Behavior : the Official Publication of the Society for Public Health Education·Joel GittelsohnLisa K Staten
Jan 11, 2007·Medical Care Research and Review : MCRR·Melanie WassermanShoou-Yih Daniel Lee
Sep 9, 2020·American Journal of Medical Genetics. Part a·Susana Isabel FerreiraFrancesco Brancati
May 18, 2020·The Journal of Pediatrics·Midhat S FarooqiJason Y Park

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