Orthopedic Conditions and Interplay with Functional Abilities and 'MECP2' Variant Subtype in Rett Syndrome Patients

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Bibliographic Details
Title: Orthopedic Conditions and Interplay with Functional Abilities and 'MECP2' Variant Subtype in Rett Syndrome Patients
Language: English
Authors: María Galán-Olleros (ORCID 0000-0001-9074-9215), Elena González-Alguacil, Víctor Soto-Insuga, María Teresa Vara-Arias, Nelmar Valentina Ortiz-Cabrera, J. Ignacio Serrano, Rosa M. Egea-Gámez, Juan José García-Peñas, Ignacio Martínez-Caballero, Salvadora Aleza Esteras, Carlota Aparicio Fernández de Gatta, Elvira Cañedo Villarroya, Daniel Clemente Garulo, Rocío Falcón Roca, Silvia Gutiérrez Priego, Blanca López Monedero, Paula Moreno Gutiérrez, Miriam Martín Mangas, Francisca Romero Andujar, Amalia Tamariz Martel
Source: Journal of Autism and Developmental Disorders. 2025 55(8):2873-2883.
Availability: Springer. Available from: Springer Nature. One New York Plaza, Suite 4600, New York, NY 10004. Tel: 800-777-4643; Tel: 212-460-1500; Fax: 212-460-1700; e-mail: customerservice@springernature.com; Web site: https://link.springer.com/
Peer Reviewed: Y
Page Count: 11
Publication Date: 2025
Document Type: Journal Articles
Reports - Research
Descriptors: Genetic Disorders, Intellectual Disability, Physical Disabilities, Patients, Children, Adolescents, Incidence
DOI: 10.1007/s10803-024-06399-y
ISSN: 0162-3257
1573-3432
Abstract: Purpose: Rett syndrome (RTT) is a rare multi-systemic disorder primarily linked to mutations in "MECP2" gene. This study aims to describe the prevalence of orthopedic conditions in RTT patients, and examine their intricate interplay with functional capabilities, and "MECP2" variant subtypes. Methods: Conducted as a cross-sectional retrospective observational study, the research encompassed 55 patients meeting clinical RTT criteria and holding "MECP2" mutations. A review of clinical records was performed to gather demographic data, mutation subtypes, orthopedic conditions, management strategies, and assessments of function. Results: Mean age of the participants was 10.22 ± 4.64 years (range, 2.9-19.41). Prevalence rates of orthopedic conditions were as follows: kyphoscoliosis 63.6%, hip displacement 14.6%, knee problems 40%, and foot deformities 75.5%. Significant relationship emerged between spinal (p < 0.01) and knee deformities (p < 0.01) with reduced motor function across various domains. Hip displacement significantly affected sitting ability (p = 0.002), and foot deformities impacted standing and walking capabilities (p = 0.049). Mutation clusters analysis revealed significant correlations with spinal (p = 0.022) and knee deformities (p = 0.002). Linear models highlighted the critical importance of mutation clusters, spine deformities, age, and hip management concerning functional variables. Conclusions: In this study, foot deformities were the most frequent orthopedic manifestation, followed by spinal, knee, and hip deformities; and unveiled their relationships with functional status and groups of mutations in RTT patients. Level of Evidence: Level IV, Case series.
Abstractor: As Provided
Entry Date: 2025
Accession Number: EJ1478301
Database: ERIC
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Abstract:Purpose: Rett syndrome (RTT) is a rare multi-systemic disorder primarily linked to mutations in "MECP2" gene. This study aims to describe the prevalence of orthopedic conditions in RTT patients, and examine their intricate interplay with functional capabilities, and "MECP2" variant subtypes. Methods: Conducted as a cross-sectional retrospective observational study, the research encompassed 55 patients meeting clinical RTT criteria and holding "MECP2" mutations. A review of clinical records was performed to gather demographic data, mutation subtypes, orthopedic conditions, management strategies, and assessments of function. Results: Mean age of the participants was 10.22 ± 4.64 years (range, 2.9-19.41). Prevalence rates of orthopedic conditions were as follows: kyphoscoliosis 63.6%, hip displacement 14.6%, knee problems 40%, and foot deformities 75.5%. Significant relationship emerged between spinal (p < 0.01) and knee deformities (p < 0.01) with reduced motor function across various domains. Hip displacement significantly affected sitting ability (p = 0.002), and foot deformities impacted standing and walking capabilities (p = 0.049). Mutation clusters analysis revealed significant correlations with spinal (p = 0.022) and knee deformities (p = 0.002). Linear models highlighted the critical importance of mutation clusters, spine deformities, age, and hip management concerning functional variables. Conclusions: In this study, foot deformities were the most frequent orthopedic manifestation, followed by spinal, knee, and hip deformities; and unveiled their relationships with functional status and groups of mutations in RTT patients. Level of Evidence: Level IV, Case series.
ISSN:0162-3257
1573-3432
DOI:10.1007/s10803-024-06399-y