Literature DB >> 22178197

Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism.

A Gulhan Ercan-Sencicek1, Nicole R Davis Wright, Stephen J Frost, Robert K Fulbright, Susan Felsenfeld, Lesley Hart, Nicole Landi, W Einar Mencl, Stephan J Sanders, Kenneth R Pugh, Matthew W State, Elena L Grigorenko.   

Abstract

Potocki-Lupski syndrome (PTLS; OMIM 610883) is a genomic syndrome that arises as a result of a duplication of 17p11.2. Although numerous cases of individuals with PTLS have been presented in the literature, its behavioral characterization is still ambiguous. We present a male child with a de novo dup(17)(p11.2p11.2) and he does not possess any autistic features, but is characterized by severe speech and language impairment. In the context of the analyses of this patient and other cases of PTLS, we argue that the central feature of the syndrome appears to be related to diminished speech and language capacity, rather than the specific social deficits central to autism. Published by Elsevier B.V.

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Year:  2011        PMID: 22178197      PMCID: PMC3343226          DOI: 10.1016/j.braindev.2011.11.003

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  10 in total

Review 1.  Clinical implications of cross-system interactions.

Authors:  David H McFarland; Pascale Tremblay
Journal:  Semin Speech Lang       Date:  2006-11       Impact factor: 1.761

2.  Three new patients with dup(17)(p11.2p11.2) without autism.

Authors:  D Greco; C Romano; S Reitano; C Barone; D D Benedetto; L Castiglia; M Fichera; O Galesi; M Zingale; S Buono; V Uliana; R Caselli; R Canitano; G Hayek; A Renieri
Journal:  Clin Genet       Date:  2008-01-23       Impact factor: 4.438

3.  Cognitive and behavioral characterization of the Potocki-Lupski syndrome (duplication 17p11.2).

Authors:  Diane E Treadwell-Deering; M Paige Powell; Lorraine Potocki
Journal:  J Dev Behav Pediatr       Date:  2010 Feb-Mar       Impact factor: 2.225

4.  Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.

Authors:  Lorraine Potocki; Weimin Bi; Diane Treadwell-Deering; Claudia M B Carvalho; Anna Eifert; Ellen M Friedman; Daniel Glaze; Kevin Krull; Jennifer A Lee; Richard Alan Lewis; Roberto Mendoza-Londono; Patricia Robbins-Furman; Chad Shaw; Xin Shi; George Weissenberger; Marjorie Withers; Svetlana A Yatsenko; Elaine H Zackai; Pawel Stankiewicz; James R Lupski
Journal:  Am J Hum Genet       Date:  2007-02-26       Impact factor: 11.025

5.  Neonatal feeding performance as a predictor of neurodevelopmental outcome at 18 months.

Authors:  Katsumi Mizuno; Aki Ueda
Journal:  Dev Med Child Neurol       Date:  2005-05       Impact factor: 5.449

6.  A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

Authors:  Santhosh Girirajan; Jill A Rosenfeld; Gregory M Cooper; Francesca Antonacci; Priscillia Siswara; Andy Itsara; Laura Vives; Tom Walsh; Shane E McCarthy; Carl Baker; Heather C Mefford; Jeffrey M Kidd; Sharon R Browning; Brian L Browning; Diane E Dickel; Deborah L Levy; Blake C Ballif; Kathryn Platky; Darren M Farber; Gordon C Gowans; Jessica J Wetherbee; Alexander Asamoah; David D Weaver; Paul R Mark; Jennifer Dickerson; Bhuwan P Garg; Sara A Ellingwood; Rosemarie Smith; Valerie C Banks; Wendy Smith; Marie T McDonald; Joe J Hoo; Beatrice N French; Cindy Hudson; John P Johnson; Jillian R Ozmore; John B Moeschler; Urvashi Surti; Luis F Escobar; Dima El-Khechen; Jerome L Gorski; Jennifer Kussmann; Bonnie Salbert; Yves Lacassie; Alisha Biser; Donna M McDonald-McGinn; Elaine H Zackai; Matthew A Deardorff; Tamim H Shaikh; Eric Haan; Kathryn L Friend; Marco Fichera; Corrado Romano; Jozef Gécz; Lynn E DeLisi; Jonathan Sebat; Mary-Claire King; Lisa G Shaffer; Evan E Eichler
Journal:  Nat Genet       Date:  2010-02-14       Impact factor: 38.330

7.  EFCBP1/NECAB1, a brain-specifically expressed gene with highest abundance in temporal lobe, encodes a protein containing EF-hand and antibiotic biosynthesis monooxygenase domains.

Authors:  Hai Wu; Dan Li; Yuxi Shan; Bo Wan; Saiyin Hexige; Jinhu Guo; Chaoqun Wu; Long Yu
Journal:  DNA Seq       Date:  2007-02

8.  Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.

Authors:  Jessica Molina; Paulina Carmona-Mora; Jacqueline Chrast; Paola M Krall; César P Canales; James R Lupski; Alexandre Reymond; Katherina Walz
Journal:  Hum Mol Genet       Date:  2008-05-10       Impact factor: 6.150

9.  Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.

Authors:  W-M Chan; E I Traboulsi; B Arthur; N Friedman; C Andrews; E C Engle
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318

10.  Analyses of beta-1 syntrophin, syndecan 2 and gem GTPase as candidates for chicken muscular dystrophy.

Authors:  Kanako Yoshizawa; Kyoko Inaba; Hideyuki Mannen; Tateki Kikuchi; Makoto Mizutani; Soichi Tsuji
Journal:  Exp Anim       Date:  2003-10
  10 in total
  5 in total

Review 1.  Neurodevelopmental Disorders Associated with Abnormal Gene Dosage: Smith-Magenis and Potocki-Lupski Syndromes.

Authors:  Juanita Neira-Fresneda; Lorraine Potocki
Journal:  J Pediatr Genet       Date:  2015-09-28

2.  Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior.

Authors:  Detlef H Heck; Wenli Gu; Ying Cao; Shuhua Qi; Melanie Lacaria; James R Lupski
Journal:  Am J Med Genet A       Date:  2012-09-18       Impact factor: 2.802

3.  A New Patient with Potocki-Lupski Syndrome: A Literature Review.

Authors:  Andrea Domenico Praticò; Raffaele Falsaperla; Renata Rizzo; Martino Ruggieri; Alberto Verrotti; Piero Pavone
Journal:  J Pediatr Genet       Date:  2017-07-27

Review 4.  Genetic insights into the functional elements of language.

Authors:  Adam Szalontai; Katalin Csiszar
Journal:  Hum Genet       Date:  2013-06-08       Impact factor: 4.132

5.  RAI1 Overexpression Promotes Altered Circadian Gene Expression and Dyssomnia in Potocki-Lupski Syndrome.

Authors:  Sureni V Mullegama; Joseph T Alaimo; Michael D Fountain; Brooke Burns; Amanda Hebert Balog; Li Chen; Sarah H Elsea
Journal:  J Pediatr Genet       Date:  2017-03-07
  5 in total

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