» Articles » PMID: 29441219

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

Overview
Journal J Pediatr Genet
Publisher Thieme
Specialty Pediatrics
Date 2018 Feb 15
PMID 29441219
Citations 9
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Potocki-Lupski Syndrome in Ethiopian Child: A Case Report.

Deginet E, Abdissa D, Hailu T Pediatric Health Med Ther. 2024; 15:129-131.

PMID: 38558960 PMC: 10981369. DOI: 10.2147/PHMT.S451161.


Family case of Potocki-Lupski syndrome.

Kolbasin L, Dubrovskaya T, Salnikova G, Solovieva E, Donnikov M, Illarionov R Mol Cytogenet. 2024; 17(1):6.

PMID: 38519962 PMC: 10960457. DOI: 10.1186/s13039-024-00673-5.


Does the Potocki-Lupski Syndrome Convey the Autism Spectrum Disorder Phenotype? Case Report and Scoping Review.

Talantseva O, Portnova G, Romanova R, Martynova D, Sysoeva O, Grigorenko E J Pers Med. 2023; 13(3).

PMID: 36983620 PMC: 10053863. DOI: 10.3390/jpm13030439.


A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele.

Sironi A, Bestetti I, Masciadri M, Tumiatti F, Crippa M, Pantaleoni C Eur J Hum Genet. 2022; 30(11):1233-1238.

PMID: 35821519 PMC: 9626456. DOI: 10.1038/s41431-022-01143-5.


Anesthesia in a Patient with Potocki-Lupski Syndrome.

Kim S, Lim Y, Jun I, Yoo B, Kim K Case Rep Anesthesiol. 2021; 2021:3313904.

PMID: 34904058 PMC: 8665889. DOI: 10.1155/2021/3313904.


References
1.
Treadwell-Deering D, Powell M, Potocki L . Cognitive and behavioral characterization of the Potocki-Lupski syndrome (duplication 17p11.2). J Dev Behav Pediatr. 2010; 31(2):137-43. DOI: 10.1097/DBP.0b013e3181cda67e. View

2.
Shuib S, Saaid N, Zakaria Z, Ismail J, Abdul Latiff Z . Duplication 17p11.2 (Potocki-Lupski Syndrome) in a child with developmental delay. Malays J Pathol. 2017; 39(1):77-81. View

3.
Ercan-Sencicek A, Davis Wright N, Frost S, Fulbright R, Felsenfeld S, Hart L . Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism. Brain Dev. 2011; 34(8):700-3. PMC: 3343226. DOI: 10.1016/j.braindev.2011.11.003. View

4.
Zhang F, Potocki L, Sampson J, Liu P, Sanchez-Valle A, Robbins-Furman P . Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS. Am J Hum Genet. 2010; 86(3):462-70. PMC: 2833368. DOI: 10.1016/j.ajhg.2010.02.001. View

5.
Loviglio M, Beck C, White J, Leleu M, Harel T, Guex N . Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics. Genome Med. 2016; 8(1):105. PMC: 5088687. DOI: 10.1186/s13073-016-0359-z. View