1.Clinical and genetic analysis of four patients with Phelan-McDermid syndrome due to variants of SHANK gene.
Liangqiong DENG ; Xuan ZENG ; Linyan LIAO ; Xiaobo XIONG ; Aiwen LI ; Yan MEI ; Liujuan ZHANG ; Dejian YUAN
Chinese Journal of Medical Genetics 2025;42(5):563-567
OBJECTIVE:
To explore the clinical phenotype and genetic characteristics of four patients with Phelan-McDermid syndrome (PMS) due to variants of SHANK3 gene.
METHODS:
Four patients diagnosed with PMS at Guangzhou Women and Children's Medical Center Liuzhou Hospital from January 2020 to January 2025 were selected as the study subjects. Clinical data of the patients were collected. Peripheral venous blood samples were collected from each patient for the extraction of genomic DNA, followed by whole-exome sequencing (WES) and validation by Sanger sequencing. Pathogenicity of candidate variants was rated based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), and multiple bioinformatic tools were used to assess the pathogenic effects of the variants. The study was approved by the Ethics Committee of the Hospital (Ethics No. 2025-007).
RESULTS:
All four patients had exhibited language delay and intellectual disability (IQ 35 ~ 65). Some also presented with autism spectrum disorder and schizophrenia, albeit with significant phenotypic heterogeneity. All patients were found to harbor deletions of 22q13.33 region, ranging from 55.46 Kb to 112.64 Kb, primarily involving the SHANK3 gene.
CONCLUSION
PMS is typically caused by deletions or mutations of the SHANK3 gene. The clinical manifestations are diverse, with developmental delay and intellectual disability being the most common. Accurate diagnosis requires integration of genetic testing and standardized clinical assessment. Genetic screening for suspected patients and at-risk pregnant women is recommended to facilitate their genetic counseling.
Child
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Humans
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Chromosome Deletion
;
Chromosome Disorders/genetics*
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Chromosomes, Human, Pair 22/genetics*
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Exome Sequencing
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Nerve Tissue Proteins/genetics*
;
Phenotype
2.Observations on the Therapeutic Effect of Acupuncture on Dyssomnia in Children with Mental Retardation
Yiyi CENG ; Renxiu HUANG ; Liangqiong DENG ; Fangjian LIU
Shanghai Journal of Acupuncture and Moxibustion 2015;(9):836-838
Objective To investigate the clinical efficacy of acupuncture in treating dyssomnia in children with mental retardation. Methods Sixty patients with mental retardation (4-6 years old) were randomly allocated to treatment and control groups, 30 cases each. The control group received routine rehabilitation therapy (family training guidance, and aetiological, psychological and behavioral intervention) and the treatment group, acupuncture in addition. Sleep latency, rapid eye movement (REM) sleep state and sleep efficiency were monitored by polysomnography in the two groups of patients. The clinical therapeutic effects were compared between the two groups. Results The total efficacy rate was 93.3%in the treatment group and 73.3%in the control group;there was a statistically significant difference between the two groups (P<0.05). There were statistically significant differences in pre-/post-treatment sleep latency, REM sleep state and sleep efficiency difference values between the treatment and control groups (P<0.05). Conclusion Acupuncture is an effective way to treat dyssomnia in children with mental retardation.

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