Neuropsychological and Language Deficits in 22q11.2 Deletion Syndrome

J Gordon Millichap; John J Millichap

doi:10.15844/pedneurbriefs-28-7-2

Neuropsychological and Language Deficits in 22q11.2 Deletion Syndrome

Pediatric Neurology Briefs

Volume 28 (2014): Issue 7

By: J Gordon Millichap and John J Millichap

Open Access

|Jul 2014

Abstract

Investigators at Bambino Genu Children's Hospital, Rome, and multiple additional centers in Italy conducted a retrospective and prospective study of clinical manifestations at diagnosis and during follow-up of 228 patients with 22q11.2 deletion syndrome.

References

Cancrini C Puliafito P Digilio MC Soresina A Martino S Rondelli R Clinical features and follow-up in patients with 22q11.2 deletion syndrome J Pediatr 2014 Jun 164 6 1475 1480.e2 10.1016/j.jpeds.2014.01.056 24657119
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Digilio MC Angioni A De Santis M Lombardo A Giannotti A Dallapiccola B Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies Clin Genet 2003 Apr 63 4 308 13 10.1016/j.jpeds.2014.01.056 12702165
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Millichap JG Neurological Syndromes : A Clinical Guide to Symptoms and Diagnosis 2013 New York Springer 279 10.1007/978-1-4614-7786-0
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-28-7-2 | Journal eISSN: 2166-6482

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Language: English

Page range: 50 - 51

Published on: Jul 1, 2014

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

DiGeorge,

Velo-Cardio-Facial,

Cono-Truncal-Anomaly-Face

© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 28 (2014): Issue 7