What is Spinal conditions?

What is Spinal conditions?

Any condition that affects the spine or the spinal cord within. The spine is the backbone or column of bones ...more »

• Spinal conditions: Any condition that affects the spine.

Spinal conditions: Introduction

Types of Spinal conditions:

Types of Spinal conditions:

• Spinal Cord Injury
• Spinal Cord Disorders
• Paralysis
• Spinal stenosis
• Scoliosis
• Adult SMA
• Ankylosing Spondylitis
• Disc Disorders
• Herniated disc
• Klippel Feil Syndrome
• Kyphosis
• Osteoarthritis
• Osteomyelitis
• Paget's disease of bone
• Progressive Spinobulbar muscular atrophy
• Reiter’s syndrome
• Scheuermann's disease
• Sciatica
• Seronegative spondyloarthropathy
• Spinal curvature
• Spinal Muscular Atrophy
• Spinal Muscular Atrophy type I
• Spinal Muscular Atrophy type II
• Spinal Muscular Atrophy type III
• Spondylitis
• Spondylosis
• Tuberculosis
• Vertebral fracture
• Arthritis
• Lordosis
• Demyelinating disorder
• Dislocation
• Adolescent idiopathic scoliosis
• Whiplash
• Broken neck
• Idiopathic adolescent scoliosis
• Cleft palate -- short stature -- vertebral anomalies
• Opthalmoplegia progressive external scoliosis
• Type I spinal osteoporosis
• Spine osteoarthritis
• Spondylolisthesis
• Scoliosis, Idiopathic, Susceptibility to, 5
• Scoliosis, Idiopathic, Susceptibility to, 4
• Scoliosis, Idiopathic, Susceptibility to, 3
• Scoliosis, Idiopathic, Susceptibility to, 2
• Scoliosis, Idiopathic, Susceptibility to, 1
• Optic-spinal form of multiple sclerosis
• Degenerative Disc Disease
• Arachnoiditis
• Arachnoid Cysts
• Swayback
• Primary osteoporosis
• Spinal pain and rigidity
• Ehlers-Danlos syndrome, 6B
• Ehlers-Danlos syndrome type VI
• Ehlers-Danlos syndrome type IX
• Ehlers-Danlos syndrome, kyphoscoliosis type
• Arnold-Chiari malformation type 2
• Osteogenesis imperfecta, type 3
• Osteogenesis imperfecta, type 4
• Osteogenesis imperfecta, type 5
• Osteogenesis imperfecta, type 6
• Osteogenesis imperfecta type IV
• Spina bifida -- hypospadias
• Microcephaly -- cervical spine fusion anomalies
• Ophthalmoplegia, progressive external -- scoliosis
• Mental retardation -- short stature -- scoliosis
• Coccyx injury
• Spinal Arthritis
• Spondylarthropathy
• Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal/Spinal abnormalities
• Sacroilitis
• Orofaciodigital syndrome, type 3
• Sugarman syndrome
• Scoliosis as part of NF
• Scoliosis with unilateral unsegmented bar
• Spondylarthritis
• Oculoauriculovertebral (OAV) dysplasia
• Goldenhar Syndrome
• Brachydactyly -- scoliosis -- carpal fusion
• Discitis
• Pena Shokeir syndrome, type 1
• Pena-Shokeir syndrome Type 2
• COFS syndrome
• Cerebro-Oculo-Facio-Skeletal Syndrome
• Arthrogryposis, distal, type 2A
• Freeman-Sheldon Syndrome
• Whistling face syndrome
• Hydrocephalus -- costovertebral dysplasia -- Sprengel anomaly
• Hydrocephaly tall stature joint laxity and kyphoscoliosis
• Ischio-vertebral syndrome
• Ischio-spinal dysostosis
• Ischio-spinal dysostosis with cystic kidney disease
• Ischio-spinal dysostosis -- rib gaps -- nephroblastomatosis
• Spondylometaphyseal dysplasia with dentinogenesis imperfecta
• Ankylosing spondylarthritis
• Cerebro-facio-thoracic dysplasia
• Myelitis
• Transverse myelitis
• Spina bifida
• Meningomyelocele
• Renal agenesis -- meningomyelocele -- mullerian defect
• Anencephaly and spina bifida X-linked
• Lipomyelomeningocele
• Meningocele
• Sacral meningocele -- conotruncal heart defects
• Sacral defect and anterior sacral meningocele
• Lateral meningocele syndrome
• Perineal hemangioma -- external genitalia malformations -- lipomyelomeningocele -- vesicorenal abnormalities -- imperforate anus
• Atlanto-Axial Fusion
• Shprintzen omphalocele syndrome
• Omphalocele -- exstrophy -- imperforate anus
• Wildervanck syndrome
• Roussy-Levy hereditary areflexic dystasia
• Cloverleaf skull micromelia thoracic dysplasia
• Polydactyly postaxial dental and vertebral
• Ossification of the posterior longitudinal ligament of the spine
• Intervertebral disc disease
• Brachial Plexus Injury
• Brown-Sequard Syndrome
• Intrathoracic kidney -- vertebral fusion
• Congenital stenosis of cervical medullary canal
• Spondyloepiphyseal dysplasia tarda, autosomal dominant
• Spondyloepiphyseal dysplasia tarda progressive arthropathy
• Spondyloepiphyseal dysplasia
• Spondyloepiphyseal dysplasia -- nephrotic syndrome
• Spondyloepiphyseal dysplasia tarda, Toledo type
• Spondyloepiphyseal dysplasia -- nephritic syndrome
• Oto-spondylo-megaepiphyseal dysplasia, autosomal recessive
• Oto-spondylo-megaepiphyseal dysplasia, homozygous
• Spondyloepiphyseal dysplasia tarda
• Spondyloepiphyseal dysplasia, congenita
• Otospondylomegaepiphyseal dysplasia
• Aphalangy -- hemivertebrae -- urogenital-intestinal dysgenesis
• Kahrizi Syndrome
• Spondyloepimetaphyseal Dysplasia, Aggrecan Type
• Spondylodysplasia and Premature Pubarche
• Spondyloepimetaphyseal Dysplasia, Pakistani Type
• Spinal AVM
• Metaphyseal undermodeling, spondylar dysplasia, and overgrowth
• Anterior horn disease
• Ischio-vertebral dysplasia
• Multiple vertebral anomalies unusual facies
• Scheuermann juvenile Kyphosis, familial
• Mirror polydactyly -- vertebral segmentation -- limbs defects
• Spinal shock
• Segmental vertebral anomalies
• Polydactyly, postaxial -- dental and vertebral anomalies
• Microsomia -- hemifacial -- radial defects
• Midline field defects
• Spondylocostal dysostosis with anal atresia and urogenital anomalies
• Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction
• Cleft lip palate -- deafness -- sacral lipoma
• Dysraphism -- cleft lip palate -- limb reduction defects
• Leg absence -- deformity -- cataract
• Night blindness -- skeletal anomalies -- unusual facies
• Caudal dysplasia sequence
• Caudal regression syndrome
• Holoprosencephaly -- caudal dysgenesis
• Caudal appendage -- deafness
• Caudal duplication
• Nevo syndrome
• Spondylocarpotarsal synostosis
• Diaphanospondylodysostosis
• Spondylohypoplasia arthrogryposis popliteal pterygium
• Achondrogenesis type 1B
• Achondrogenesis type 1A and 1B
• Goodman camptodactyly
• Spondylo camptodactyly syndrome
• Tel-Hashomer camptodactyly syndrome
• Syncamptodactyly -- scoliosis
• Camptodactyly syndrome, Guadalajara type III
• Camptodactyly syndrome, Guadalajara type 3
• Camptodactyly -- vertebral fusion
• Larsen-like syndrome, lethal form
• Larsen-like syndrome, lethal type
• Acromesomelic dysplasia
• VATER association
• Spondyloepimetaphyseal dysplasia, hypotrichosis
• Spondylometaphyseal dysplasia -- cone-rod dystrophy
• Spondylometaphyseal dysplasia, axial
• Spondylometaphyseal dysplasia, Algerian type
• Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
• Spondylometaphyseal dysplasia, east-African type
• Spondylometaphyseal dysplasia, Sedaghatian type
• Spondylometaphyseal dysplasia, 'corner fracture' type
• Spondylometaphyseal dysplasia, Kozlowski type
• Spondylometaphyseal dysplasia with combined immunodeficiency
• Spondylometaphyseal dysplasia, X-linked
• VACTERL with hydrocephalus, X-linked
• VACTERL association
• VACTERYL hydrocephaly
• VACTERL association with hydrocephaly, X-linked
• Thanatophoric dysplasia, type 2
• Thanatophoric dysplasia, type 1
• Spinal intradural arachnoid cysts
• Spondylocostal dysostosis, autosomal recessive 3
• Spondylocostal dysostosis, autosomal recessive 1
• Spondylocostal dysostosis, autosomal recessive 2
• Craniofaciocervical osteoglyphic dysplasia
• Rudd-Klimek syndrome
• Spinal dysostosis, type Anhalt
• Spondylohypoplasia, arthrogryposis and popliteal pterygium
• Skeletal dysplasia, San Diego type
• Spondyloepimetaphyseal dysplasia with joint laxity
• Spondylocostal dysostosis, autosomal recessive
• Spondylocostal dysplasia dominant
• Spondyloepimetaphyseal dysplasia, micromelic
• Spondyloepimetaphyseal dysplasia congenita, Iraqi
• Skeletal dysplasia -- coarse facies -- mental retardation
• Platyspondylic lethal chondrodysplasia
• Platyspondylic lethal skeletal dysplasia, Torrance type
• Acrodysplasia scoliosis
• Acropectorovertebral dysplasia
• Acromesomelic dysplasia, Maroteaux type
• Alves Castelo dos Santos syndrome
• Spondylo-humero-femoral dysplasia
• Microcephaly brachydactyly kyphoscoliosis
• Hunter-MacDonald syndrome
• Dysspondyloenchondromatosis
• Vertebral Artery Dissection
• Lumbar malsegmentation, short stature and facial anomalies
• Vertebral body fusion overgrowth
• Vertebral fusion posterior lumbosacral blepharoptosis
• Cervical Spondylosis
• Spondylo-ocular syndrome
• Sketetal dysplasia coarse facies mental retardation
• Spondyloenchondrodysplasia
• Kozlowski Celermajer Tink syndrome
• Intellectual deficit -- multiple anomalies
• Facet syndrome
• Robinson syndrome
• Goldenhar disease
• Schwartz newark syndrome
• Schanz disease
• Schanz's syndrome
• Seven point syndrome
• Turpin syndrome
• Zanoli-Vecchi syndrome
• Spondyloepimetaphyseal dysplasia, genevieve type
• Verloes-Deprez syndrome
• Whistling face syndrome, recessive form
• Kashin-Bek disease
• CAMFAK syndrome
• Jaffer-Beighton syndrome
• Fibrocartilaginous embolism
• Escobar syndrome, type B
• Basilar impression primary
• Fryns-Fabry-Remans syndrome
• Iida-Kannari syndrome
• Hypoplasia hepatic ductular
• Kozlowski-Celermajer syndrome
• Johnson-Munson syndrome
• Bartenwerfer syndrome
• Breakdance back syndrome
• Dreyfus syndrome
• Golden-Lakin syndrome
• Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
• Michels-Caskey syndrome
• Laplane-Fontaine-Lagardere syndrome
• Melhem-Fahl syndrome
• Spondylocostal dysostosis, Dandy-Walker
• Ghosal syndrome
• Sacral hemangiomas -- multiple congenital abnormalities
• Spondyloepimetaphyseal dysplasia, X linked with mental deterioration
• Spondyloepimetaphyseal dysplasia, Missouri type
• Spondyloepimetaphyseal dysplasia with multiple dislocations
• Diphallus -- rachischisis -- imperforate anus
• Czeizel-Losonci syndrome
• Spondyloepimetaphyseal dysplasia, X-linked
• Spondyloepimetaphyseal dysplasia, Irapa type
• Kozlowski-Brown-Hardwick syndrome
• Ray-Peterson-Scott syndrome
• Spondyloperipheral dysplasia -- short ulna
• Spondyloepimetaphyseal dysplasia joint laxity
• Powell-Chandra-Saal syndrome
• Sacrococcygeal dysgenesis association
• McDonough syndrome
• Seghers syndrome
• Vertebral fusion- posterior lumbrosacral, blepharoptosis
• Kasznica-Carlson-Coppedge syndrome
• Spondyloepimetaphyseal dysplasia with hypotrichosis
• Tsukuhara syndrome
• Colver-Steer-Godman syndrome
• Tarlov cysts
• Rosenberg-Lohr syndrome
• Dysosteosclerosis
• Brachyrachia
• Bazopoulou-Kyrkanidou syndrome
• Beardwell syndrome
• Sacral agenesis
• Game-Friedman-Paradice syndrome
• Saul-Wilkes-Stevenson syndrome
• Desbuquois syndrome
• Verloes Bourguignon syndrome
• Waaler Aarskog syndrome
• Currarino triad
• Sillence syndrome
• Parastremmatic dwarfism
• Barre-Lieou syndrome
• King-Denborough syndrome
• Sponastrime dysplasia
• Occult spinal dysraphism
• Cervicooculoacoustic syndrome
• Aneurysmal bone cysts
• Pycnodysostosis
• Venencie Powell Winkelmann syndrome
• more types...»

Broader types of Spinal conditions:

• Back conditions
• Neck conditions
• Musculoskeletal conditions
• Senior health conditions
• more types...»

What causes Spinal conditions?

Causes of Spinal conditions: see causes of Spinal conditions

What are the symptoms of Spinal conditions?

Symptoms of Spinal conditions: see symptoms of Spinal conditions

Spinal conditions: Testing

Misdiagnosis: see misdiagnosis and Spinal conditions.

How is it treated?

Doctors and Medical Specialists for Spinal conditions: Orthopedic Surgeon, Family Practice Physician, Neurologist, Physiatrist ; see also doctors and medical specialists for Spinal conditions.
Treatments for Spinal conditions: see treatments for Spinal conditions
Research for Spinal conditions: see research for Spinal conditions

Society issues for Spinal conditions

Hospitalization statistics for Spinal conditions: The following are statistics from various sources about hospitalizations and Spinal conditions:

• 1.26% (160,585) of hospital episodes were for dorsopathies in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• 95% of hospital consultations for dorsopathy required hospital admission in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• 42% of hospital episodes for dorsopathies were for men in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• 58% of hospital episodes for dorsopathies were for women in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• 20% of hospital admissions for dorsopathy required emergency hospital admission in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• 7.5 days was the mean length of stay in hospitals for dorsopathies in England 2002-03 (Hospital Episode Statistics, Department of Health, England, 2002-03)
• more statistics...»

Organs Affected by Spinal conditions:

Organs and body systems related to Spinal conditions include:

• Spine

Name and Aliases of Spinal conditions

Main name of condition: Spinal conditions

Spinal disorders, Spinal diseases, Spine conditions, Spine diseases

Spinal conditions: Related Conditions

Research the causes of these diseases that are similar to, or related to, Spinal conditions:

• Peripheral neuropathy
• Bone fracture
• Nerve injury
• Diabetes
• Spinal cord diseases
• Slipped disc

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