Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Nonidiopathic Types, Understanding and managing the condition: A practical guide for familiesBy Tenner J.Guillaume, Walter H.Truong, DanielleHarding, LilyCollison, and CherylTveitGillette Chi

The authors introduce the three-dimensional nature of spine pathoanatomy, where the deformity occurs in all three anatomic planes involving different functional and structural regions of the spine (cervical, thoracic, lumbar, and sacrum/pelvis). Scoliosis is the projection of the deformity onto the coronal plane, kyphosis/lordosis is the projection of the deformity onto the sagittal plane, and torsion/rotation is the projection of the deformity onto the axial plane. Spine development is examined from in utero to skeletal maturity, highlighting how the pubertal growth spurt accelerates deformity progression in adolescence, and also considers issues of adults with distorted spines during aging. The authors explain how spine deformity is classified according to the cause (congenital, neuromuscular, syndromic, or non-idiopathic spinal cord malformations) and age at onset (early – infantile or juvenile and later – adolescent). Common signs and symptoms of spine pathoanatomy that parents and care providers should notice are outlined and the importance of timely referral to a spine specialist is emphasized. Creating an effective treatment plan is predicated on a comprehensive medical history, physical exam, and imaging studies that includes multi-planar spine radiographs with or without magnetic resonance imaging to visualize all relevant musculoskeletal pathology. For each category of spine deformity, the book is structured to guide readers through the various treatment modalities, the selection based on the underlying diagnosis, patient age, anatomic location, severity of deformity, and coexisting medical comorbidities. Chapters 6 through 9 are dedicated to an overview of therapies, covering both nonsurgical options (observation, bracing, casting, physical therapy, alternative treatments) and surgical interventions (spinal fusion, growth-friendly spine instrumentation, halo gravity traction). Chapter 9 delves into specific considerations relevant to congenital, neuromuscular, syndromic, or non-idiopathic cord abnormalities. A unique aspect of this book is the inclusion of the lived experiences of children with scoliosis and their families. Complementing the didactic medical information, personal stories are interspersed throughout the text, offering a human dimension to this disorder. Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Nonidiopathic Types serves as a vital educational resource for patients, their families, and healthcare professionals alike, emphasizing evidence-based best practices and providing guidance for exploring the literature and further research. Beyond the pragmatic medical information provided, the text underscores the critical partnerships among patients, their families/caretakers, and healthcare professionals in optimizing outcomes for individuals living with this lifelong condition. Not required.

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Publication Details

Journal
Developmental Medicine & Child Neurology
Published
2025-10-31
DOI
https://doi.org/10.1111/dmcn.70054
Primary Topic
Scoliosis diagnosis and treatment
Type
article
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article

Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Nonidiopathic Types, Understanding and managing the condition: A practical guide for familiesBy Tenner J.Guillaume, Walter H.Truong, DanielleHarding, LilyCollison, and CherylTveitGillette Chi

Brian Snyder
Developmental Medicine & Child Neurology
Scoliosis diagnosis and treatment
article

Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Nonidiopathic Types, Understanding and managing the condition: A practical guide for familiesBy Tenner J.Guillaume, Walter H.Truong, DanielleHarding, LilyCollison, and CherylTveitGillette Chi

Brian Snyder
article en

Abstract

The authors introduce the three-dimensional nature of spine pathoanatomy, where the deformity occurs in all three anatomic planes involving different functional and structural regions of the spine (cervical, thoracic, lumbar, and sacrum/pelvis). Scoliosis is the projection of the deformity onto the coronal plane, kyphosis/lordosis is the projection of the deformity onto the sagittal plane, and torsion/rotation is the projection of the deformity onto the axial plane. Spine development is examined from in utero to skeletal maturity, highlighting how the pubertal growth spurt accelerates deformity progression in adolescence, and also considers issues of adults with distorted spines during aging. The authors explain how spine deformity is classified according to the cause (congenital, neuromuscular, syndromic, or non-idiopathic spinal cord malformations) and age at onset (early – infantile or juvenile and later – adolescent). Common signs and symptoms of spine pathoanatomy that parents and care providers should notice are outlined and the importance of timely referral to a spine specialist is emphasized. Creating an effective treatment plan is predicated on a comprehensive medical history, physical exam, and imaging studies that includes multi-planar spine radiographs with or without magnetic resonance imaging to visualize all relevant musculoskeletal pathology. For each category of spine deformity, the book is structured to guide readers through the various treatment modalities, the selection based on the underlying diagnosis, patient age, anatomic location, severity of deformity, and coexisting medical comorbidities. Chapters 6 through 9 are dedicated to an overview of therapies, covering both nonsurgical options (observation, bracing, casting, physical therapy, alternative treatments) and surgical interventions (spinal fusion, growth-friendly spine instrumentation, halo gravity traction). Chapter 9 delves into specific considerations relevant to congenital, neuromuscular, syndromic, or non-idiopathic cord abnormalities. A unique aspect of this book is the inclusion of the lived experiences of children with scoliosis and their families. Complementing the didactic medical information, personal stories are interspersed throughout the text, offering a human dimension to this disorder. Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Nonidiopathic Types serves as a vital educational resource for patients, their families, and healthcare professionals alike, emphasizing evidence-based best practices and providing guidance for exploring the literature and further research. Beyond the pragmatic medical information provided, the text underscores the critical partnerships among patients, their families/caretakers, and healthcare professionals in optimizing outcomes for individuals living with this lifelong condition. Not required.

Developmental Medicine & Child NeurologyVol. 68(2)
Boston Children's Hospital (US), Boston Children's Museum (US)
Openalex Percentile: Top 50%
Scoliosis diagnosis and treatment
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