Functional Independence of Taiwanese Children with Silver–Russell Syndrome

<b>Background:</b> Silver-Russell syndrome (SRS) is a genetic disorder characterized by prenatal and postnatal growth retardation. Affected individuals commonly present with low birth weight, intrauterine growth restriction, postnatal short stature, hemihypotrophy, characteristic facial features, and body asymmetry. <b>Methods:</b> This study includes 24 Taiwanese children with SRS aged 2 years to 13 years and 3 months who were recruited at MacKay Memorial Hospital and other Taiwan hospitals between January 2013 and December 2024. Functional independence was assessed using the Functional Independence Measure for Children (WeeFIM) to evaluate self-care, mobility, and cognition domains. <b>Results:</b> The mean total WeeFIM score was 106.9 ± 23.2 (range: 54-126), with mean self-care, mobility, and cognition scores of 44.4 ± 13.8 (maximum 56), 32.4 ± 5.1 (maximum 35), and 30.2 ± 6.0 (maximum 35), respectively. The results of the restricted cubic spline analysis reveal a clear positive linear correlation before school age (approximately 72 months), followed by a plateau (<i>p</i> for nonlinearity < 0.05). Traceable molecular data were available for thirteen participants, of whom nine (69%) had loss of methylation at chromosome 11p15 (11p15LOM), and four (31%) had maternal uniparental disomy of chromosome 7 (upd(7)mat). Of the 24 children, 46% required assistance with bathing, which was strongly correlated with self-care ability and body height. In contrast, most of the children had independence in mobility tasks such as walking and stair climbing. However, some required support in cognitive tasks, including problem-solving, comprehension, and expression. Overall, the included children reached a functional plateau later than the normative population, with the greatest delays in self-care and mobility domains. <b>Conclusions:</b> This study highlights that Taiwanese children with SRS require support in self-care and cognitive tasks. Functional independence in self-care and mobility domains was positively associated with body height. The WeeFIM questionnaire effectively identified strengths and limitations, emphasizing the need for individualized support in daily activities.

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Journal
Diagnostics
Published
2025-04-27
DOI
https://doi.org/10.3390/diagnostics15091109
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
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article

Functional Independence of Taiwanese Children with Silver–Russell Syndrome

Chung‐Hsing Wang, Chen Yang, Tsung-Ying Ou, Hsiang‐Yu Lin et al.
Diagnostics
Genetic Syndromes and Imprinting
article

Functional Independence of Taiwanese Children with Silver–Russell Syndrome

Chung‐Hsing Wang, Chen Yang, Tsung-Ying Ou, Hsiang‐Yu Lin, Yuan-Rong Tu, Chung‐Lin Lee, Yen‐Yin Chou, Shuan‐Pei Lin, Shao‐Yin Chu, Hung‐Hsiang Fang, Chih‐Kuang Chuang, Junyi Wu, Huei‐Ching Chiu, Yun‐Ting Lo, Ya-Hui Chang, Shio‐Jean Lin
article en

Abstract

<b>Background:</b> Silver-Russell syndrome (SRS) is a genetic disorder characterized by prenatal and postnatal growth retardation. Affected individuals commonly present with low birth weight, intrauterine growth restriction, postnatal short stature, hemihypotrophy, characteristic facial features, and body asymmetry. <b>Methods:</b> This study includes 24 Taiwanese children with SRS aged 2 years to 13 years and 3 months who were recruited at MacKay Memorial Hospital and other Taiwan hospitals between January 2013 and December 2024. Functional independence was assessed using the Functional Independence Measure for Children (WeeFIM) to evaluate self-care, mobility, and cognition domains. <b>Results:</b> The mean total WeeFIM score was 106.9 ± 23.2 (range: 54-126), with mean self-care, mobility, and cognition scores of 44.4 ± 13.8 (maximum 56), 32.4 ± 5.1 (maximum 35), and 30.2 ± 6.0 (maximum 35), respectively. The results of the restricted cubic spline analysis reveal a clear positive linear correlation before school age (approximately 72 months), followed by a plateau (<i>p</i> for nonlinearity < 0.05). Traceable molecular data were available for thirteen participants, of whom nine (69%) had loss of methylation at chromosome 11p15 (11p15LOM), and four (31%) had maternal uniparental disomy of chromosome 7 (upd(7)mat). Of the 24 children, 46% required assistance with bathing, which was strongly correlated with self-care ability and body height. In contrast, most of the children had independence in mobility tasks such as walking and stair climbing. However, some required support in cognitive tasks, including problem-solving, comprehension, and expression. Overall, the included children reached a functional plateau later than the normative population, with the greatest delays in self-care and mobility domains. <b>Conclusions:</b> This study highlights that Taiwanese children with SRS require support in self-care and cognitive tasks. Functional independence in self-care and mobility domains was positively associated with body height. The WeeFIM questionnaire effectively identified strengths and limitations, emphasizing the need for individualized support in daily activities.

DiagnosticsVol. 15(9)
Fu Jen Catholic University (TW), Tri-Service General Hospital (TW), National Yang Ming Chiao Tung University (TW), China Medical University (TW), National Taipei University of Nursing and Health Science (TW), Taipei Medical University Hospital (TW), Mackay Memorial Hospital (TW), Mackay Medical University (TW), Buddhist Tzu Chi General Hospital (TW), China Medical University Hospital (TW), Mackay Junior College of Medicine, Nursing and Management (TW), Chi Mei Medical Center (TW), National Cheng Kung University Hospital (TW), National Defense Medical Center (TW)
Mackay Memorial Hospital, National Science and Technology Council
Openalex Percentile: Top 90%
Genetic Syndromes and Imprinting
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