Literature DB >> 29441219

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

Andrea Domenico Praticò1,2, Raffaele Falsaperla3, Renata Rizzo1, Martino Ruggieri1, Alberto Verrotti4, Piero Pavone3.   

Abstract

Speech delay, intellectual disability, and behavioral disturbances are the main clinical manifestations of Potocki-Lupski syndrome. Other features include infantile hypotonia, the absence of major dysmorphism, sleep disorders, and congenital anomalies, particularly of the cardiovascular system. A male patient with Potocki-Lupski syndrome is reported herein. He showed speech and borderline cognitive delay, behavioral troubles with no signs suggestive of autism, in the absence of major dysmorphism. A de novo 17p12-p11.2 duplication spanning 3.6 Mb was detected, with boundaries from 15,284,052 to 18,647,233 (hg19 assembly). At the age of 5 years, the child showed a noticeable improvement of speech skills and a moderate scholastic performance was reached. Upon analysis of the clinical manifestations of the present patient and those reported in existing literature, we found that the syndrome may present in various degrees of clinical expressivity. Affected patients may manifest symptoms ranging from mild behavioral disturbances to severe degrees of autism.

Entities:  

Keywords:  Potocki–Lupski syndrome; autism; behavioral disturbances; cognitive delay

Year:  2017        PMID: 29441219      PMCID: PMC5809167          DOI: 10.1055/s-0037-1604479

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  21 in total

1.  Potocki-Lupski syndrome: an inherited dup(17)(p11.2p11.2) with hypoplastic left heart.

Authors:  Roman Yusupov; Amy E Roberts; Ronald V Lacro; Mary Sandstrom; Azra H Ligon
Journal:  Am J Med Genet A       Date:  2011-02       Impact factor: 2.802

2.  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

3.  Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS.

Authors:  Feng Zhang; Lorraine Potocki; Jacinda B Sampson; Pengfei Liu; Amarilis Sanchez-Valle; Patricia Robbins-Furman; Alicia Delicado Navarro; Patricia G Wheeler; J Edward Spence; Campbell K Brasington; Marjorie A Withers; James R Lupski
Journal:  Am J Hum Genet       Date:  2010-02-25       Impact factor: 11.025

Review 4.  Inherited dup(17)(p11.2p11.2): expanding the phenotype of the Potocki-Lupski syndrome.

Authors:  Pilar L Magoulas; Pengfei Liu; Violet Gelowani; Claudia Soler-Alfonso; Emma C Kivuva; James R Lupski; Lorraine Potocki
Journal:  Am J Med Genet A       Date:  2013-12-05       Impact factor: 2.802

5.  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

6.  Duplication 17p11.2 (Potocki-Lupski Syndrome) in a child with developmental delay.

Authors:  S Shuib; N N Saaid; Z Zakaria; J Ismail; Z Abdul Latiff
Journal:  Malays J Pathol       Date:  2017-04       Impact factor: 0.656

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

Authors:  A Gulhan Ercan-Sencicek; 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
Journal:  Brain Dev       Date:  2011-12-16       Impact factor: 1.961

8.  Reciprocal deletion and duplication of 17p11.2-11.2: Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome.

Authors:  Cha Gon Lee; Sang-Jin Park; Jun-No Yun; Shin-Young Yim; Young Bae Sohn
Journal:  J Korean Med Sci       Date:  2012-12-07       Impact factor: 2.153

9.  Clinical and cytogenetic features of a Potocki-Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1.

Authors:  Cha Gon Lee; Sang-Jin Park; Shin-Young Yim; Young Bae Sohn
Journal:  Brain Dev       Date:  2012-10-15       Impact factor: 1.961

10.  Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.

Authors:  Maria Nicla Loviglio; Christine R Beck; Janson J White; Marion Leleu; Tamar Harel; Nicolas Guex; Anne Niknejad; Weimin Bi; Edward S Chen; Isaac Crespo; Jiong Yan; Wu-Lin Charng; Shen Gu; Ping Fang; Zeynep Coban-Akdemir; Chad A Shaw; Shalini N Jhangiani; Donna M Muzny; Richard A Gibbs; Jacques Rougemont; Ioannis Xenarios; James R Lupski; Alexandre Reymond
Journal:  Genome Med       Date:  2016-11-01       Impact factor: 11.117

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  3 in total

1.  SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis.

Authors:  Hailong Huang; Meiying Cai; Yan Wang; Bin Liang; Na Lin; Liangpu Xu
Journal:  Risk Manag Healthc Policy       Date:  2021-01-27

2.  Case report: Spinal anesthesia for cesarean section in a parturient with Potocki-Lupski syndrome.

Authors:  Junfeng Li; Jie Bao; Di Zhang; Shuzhen Zhou
Journal:  BMC Anesthesiol       Date:  2021-09-07       Impact factor: 2.217

3.  Anesthesia in a Patient with Potocki-Lupski Syndrome.

Authors:  Songhyun Kim; Yunhee Lim; In-Jung Jun; Byunghoon Yoo; Kye-Min Kim
Journal:  Case Rep Anesthesiol       Date:  2021-12-04
  3 in total

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