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Causes of Lordosis
List of causes of Lordosis
Following is a list of causes or underlying conditions (see also Misdiagnosis of underlying causes of Lordosis) that could possibly cause Lordosis includes:
- Pregnancy
- Obesity
- Prolapsed disc
- Osteoarthritis
- Spinal arthritis
- Spondylohypoplasia, arthrogryposis and popliteal pterygium - lordosis
- Short limb dwarf lethal, Mcalister Crane type - lordosis
- Limb-girdle muscular dystrophy type 2E - lordosis
- Epimetaphyseal skeletal dysplasia - lordosis
- Chromosome 9, trisomy 9p - lordosis
- Verloes Van Maldergem Marneffe syndrome - Lordosis
- Spondylocarpotarsal synostosis - lordosis
- Limb-girdle muscular dystrophy type 2F - lordosis
- Dyggve-Melchior-Clausen Syndrome - lordosis
- Bartenwerfer syndrome - lordosis
- Tel-Hashomer camptodactyly syndrome - lordosis
- Spondyloepiphyseal dysplasia - nephrotic syndrome - lordosis
- Spondyloenchondrodysplasia - lumbar lordosis
- Skeletal dysplasia, San Diego type - lordosis
- Sandhaus Ben-Ami syndrome - lordosis
- Pseudoachondroplasia - lumbar lordosis
- Platyspondylic lethal skeletal dysplasia, Torrance type - lordosis
- Hypothyroidism - dermoid cyst - cleft palate - lordosis
- Becker Muscular Dystrophy - Lumbar lordosis
- Spondylolisthesis
- Discitis
- Von Gierke disease IA - lumbar lordosis
- Strudwick syndrome - lordosis
- Spondyloepiphyseal dysplasia, congenita - lumbar lordosis
- Spondyloepimetaphyseal dysplasia congenita, Iraqi - lumbar lordosis
- Emerinopathy - lordosis
- Acroosteolysis neurogenic - lordosis
- Spondyloepimetaphyseal dysplasia, hypotrichosis - lordosis
- Rhizomelic dysplasia Patterson Lowry type - lordosis
- Nonkeratan-sulfate-excreting Morquio syndrome - lordosis
- Multiple endocrine neoplasia type 2b - lordosis
- Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia - lumbar lordosis
- Duchenne Muscular Dystrophy - lordosis
- Cartilage-hair hypoplasia-like syndrome - lumbar lordosis
- Bowing of long bones congenital - lordosis
- Trichodermodysplasia - dental alterations - lordosis
- Stiff-Person Syndrome - lordosis
- Shprintzen omphalocele syndrome - lordosis
- Osteochondrodysplatic dwarfism - deafness - retinitis pigmentosa - lordosis
- Hypochondroplasia - lumbar lordosis
- Taurodontism and disproportionate short stature - lumbar lordosis
- Superior mesenteric artery syndrome - lordosis
- Satoyoshi syndrome - lordosis
- Muscular dystrophy, Duchenne and Becker type - lordosis
- Microbrachycephaly - ptosis - cleft lip - lordosis
- McKusick type metaphyseal chondrodysplasia - lumbar lordosis
- Kashin-Bek disease - lordosis
- Hypomelanosis of Ito - lordosis
- Acromesomelic dysplasia - lumbar lordosis
- 47,XXX syndrome - lordosis
- Osteoporosis
- Achondroplasia - lordosis
- Thoracolimb dysplasia, Rivera type - lordosis
- Pseudoachondroplastic dysplasia 2 - lordosis
- Metaphyseal chondrodysplasia, recessive type - lordosis
- Lipidosis with triglyceride storage disease - lordosis
- Emanuel syndrome - lordosis
- Sponastrime dysplasia - lumbar lordosis
- Pelvic-shoulder dysplasia - lordosis
- Larsen syndrome - lordosis
- Jarcho-Levin Syndrome - lordosis
- Emery-Dreifuss muscular dystrophy, X-linked - lumbar lordosis
- Chromosome 15 inverted duplication - lordosis
- Acromesomelic dysplasia, Maroteaux type - lordosis
- Williams Syndrome - lordosis
- Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism - lordosis
- Sarcoglycanopathy - lordosis
- Muscular Dystrophy - lordosis
- Multicore disease - lordosis
- Microcephaly - cervical spine fusion anomalies - lordosis
- Mental retardation - myopathy - short stature - endocrine defect - lordosis
- Limb-girdle muscular dystrophy type 2C - lordosis
- Leg absence - deformity - cataract - lordosis
- Glycogenosis type 2 - lordosis
- Glycogen storage disease type 2 - lordosis
- Enchondromatosis-dwarfism-deafness - lordosis
- Ehlers-Danlos syndrome, classic type - lordosis
- Cohen Syndrome - lumbar lordosis
- Limb-girdle muscular dystrophy type 2D - lordosis
- Cold-induced sweating syndrome 2 - lumbar lordosis
- Chromosome 14q, proximal duplication - lordosis
- Kyphosis
More causes: see full list of causes for Lordosis
Lordosis as a symptom:
Conditions listing Lordosis as a symptom may also be potential underlying causes of Lordosis. Our database lists the following as having Lordosis as a symptom of that condition:
- 47,XXX syndrome
- Achondroplasia
- Acromesomelic dysplasia, Maroteaux type
- Acroosteolysis neurogenic
- Bartenwerfer syndrome
- Bowing of long bones congenital
- Chromosome 14q, proximal duplication
- Chromosome 15 inverted duplication
- Chromosome 9, trisomy 9p
- Duchenne Muscular Dystrophy
- Dyggve-Melchior-Clausen Syndrome
- Ehlers-Danlos syndrome, classic type
- Emanuel syndrome
- Emerinopathy
- Enchondromatosis-dwarfism-deafness
- Epimetaphyseal skeletal dysplasia
- Glycogen storage disease type 2
- Glycogenosis type 2
- Hypomelanosis of Ito
- Hypothyroidism - dermoid cyst - cleft palate
- Jarcho-Levin Syndrome
- Kashin-Bek disease
- Larsen syndrome
- Leg absence - deformity - cataract
- Limb-girdle muscular dystrophy type 2C
- Limb-girdle muscular dystrophy type 2D
- Limb-girdle muscular dystrophy type 2E
- Limb-girdle muscular dystrophy type 2F
- Lipidosis with triglyceride storage disease
- Mental retardation - myopathy - short stature - endocrine defect
- Metaphyseal chondrodysplasia, recessive type
- Microbrachycephaly - ptosis - cleft lip
- Microcephaly - cervical spine fusion anomalies
- Multicore disease
- Multiple endocrine neoplasia type 2b
- Muscular Dystrophy
- Muscular dystrophy, Duchenne and Becker type
- Muscular dystrophy, limb-girdle, autosomal recessive, type 2E
- Nonkeratan-sulfate-excreting Morquio syndrome
- Osteochondrodysplatic dwarfism - deafness - retinitis pigmentosa
- Pelvic-shoulder dysplasia
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Pseudoachondroplastic dysplasia 2
- Rhizomelic dysplasia Patterson Lowry type
- Sandhaus Ben-Ami syndrome
- Sarcoglycanopathy
- Satoyoshi syndrome
- Short limb dwarf lethal, Mcalister Crane type
- Shprintzen omphalocele syndrome
- Skeletal dysplasia, San Diego type
- Spondylocarpotarsal synostosis
- Spondyloepimetaphyseal dysplasia, hypotrichosis
- Spondyloepiphyseal dysplasia - nephrotic syndrome
- Spondylohypoplasia arthrogryposis popliteal pterygium
- Spondylohypoplasia, arthrogryposis and popliteal pterygium
- Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
- Stiff-Person Syndrome
- Strudwick syndrome
- Superior mesenteric artery syndrome
- Tel-Hashomer camptodactyly syndrome
- Thoracolimb dysplasia, Rivera type
- Trichodermodysplasia - dental alterations
- Verloes Van Maldergem Marneffe syndrome
- Williams Syndrome
Related information on causes of Lordosis:
As with all medical conditions, there may be many causal factors. Further relevant information on causes of Lordosis may be found in:
Causes of Lordosis: Online Medical Books
16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about the causes of Lordosis.
Scoliosis & Kyphosis:
Differential Diagnosis
(In a Page: Signs and Symptoms)
Scoliosis
- Idiopathic (75–80% of cases) scoliosis usually occurs in otherwise healthy patients; pain and neurologic deficits are rare; right thoracic curve is most common, then double curve (right thoracic and left lumbar); named by convex side
–Infantile (birth to 3 years): Rare in the U.S.
–Juvenile (4–10 years): Uncommon
–Adolescent (11 years to skeletal maturity): Occurs mostly in females
-
Neuromuscular scoliosis
–Common with paralytic disorders
–More severe, almost always progressive -
Congenital scoliosis
–Failure of formation or segmentation - Postural roundback
-
Scheuermann's disease
–Second most common pediatric spinal deformity
–Cannot voluntarily correct
–Angulation in mid- to low-thoracic spine -
Congenital kyphosis
Less common etiologies (“zebras”) - Post-thoracotomy
- Marfan's syndrome
- Neurofibromatosis
- Achondroplasia
- Diastrophic dwarfism
- Specific neuromuscular disorders (e.g., cerebral palsy, syringomyelia, polio, muscular dystrophy, cord tumor/trauma)
Kyphosis
Source: In a Page: Signs and Symptoms, 2004
Scoliosis:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
-
Idiopathic scoliosis
–Lateral deviation or curvature of either the thoracic or lumbar spine greater than 10°
–Right thoracic curves are most common
–Usually presents in early adolescence
–Girls > boys -
Risk factors for progression
–Curve >20°
–Age less than 12
–Skeletal maturity, Risser stage 0–1 -
Infantile idiopathic scoliosis
–Presents at 0–3 years old
–Left thoracic curve more common
–Boys > girls
–85% spontaneously resolve
–Must rule out spinal cord disease or congenital cause of scoliosis - Juvenile idiopathic scoliosis presents at 3–10 years old and is similar to adolescent (idiopathic) scoliosis
- Neuromuscular scoliosis
–Related to cerebral palsy, muscular dystrophy, myotonic myopathy, and spinal muscular atrophy
–Tends to progress more rapidly and even continues after maturity, as compared to idiopathic scoliosis
–Pulmonary complications seen with severe curves >90°
-
Congenital scoliosis
–Failure of formation or segmentation of spinal vertebra
–Rapid progression and worse prognosis is associated with unilateral unsegmented bar with contralateral hemivertebra -
Other causes
–Tumor, infection, neurofibromatosis, metabolic bone disorders, and Marfan syndrome
Source: In A Page: Pediatric Signs and Symptoms, 2007
Scoliosis:
Causes and incidence
(Professional Guide to Diseases (Eighth Edition))
Scoliosis may be functional, structural, or idiopathic. Functional (postural) scoliosis usually results from a discrepancy in leg lengths rather than from a fixed deformity of the spinal column; it corrects when the patient bends toward the convex side. Structural scoliosis results from a deformity of the vertebral bodies, and it doesn’t correct when the patient bends to the side. Structural scoliosis may be:
❑ congenital: usually related to a congenital defect, such as wedge vertebrae, fused ribs or vertebrae, or hemivertebrae; may result from trauma to zygote or embryo
❑ paralytic or musculoskeletal: develops several months after asymmetrical paralysis of the trunk muscles due to polio, cerebral palsy, or muscular dystrophy
❑ idiopathic (the most common form): may be transmitted as an autosomal dominant or multifactorial trait. This form appears in a previously straight spine during the growing years. Brain stem dysfunction, possibly due to a lesion of the posterior columns or the inner ear, may be the cause.
Idiopathic scoliosis can be classified as infantile, which affects mostly male infants between birth and age 3 and causes left thoracic and right lumbar curves; juvenile, which affects both sexes between ages 4 and 10 and causes varying types of curvature; or adolescent, which generally affects girls between age 10 and achievement of skeletal maturity and causes varying types of curvature.
Source: Professional Guide to Diseases (Eighth Edition), 2005
Scoliosis:
Causes
(Handbook of Diseases)
Scoliosis may be functional or structural. Functional (postural) scoliosis usually results from poor posture or a discrepancy in leg lengths, not fixed deformity of the spinal column. In structural scoliosis, curvature results from a deformity of the vertebral bodies.
Structural scoliosis may be one of three types:
❑ Congenital scoliosis is usually related to a congenital defect, such as wedge vertebrae, fused ribs or vertebrae, or hemivertebrae.
❑ Paralytic or musculoskeletal scoliosis develops several months after asymmetrical paralysis of the trunk muscles from polio, cerebral palsy, or muscular dystrophy.
❑ Idiopathic scoliosis (the most common form) may be transmitted as an autosomal dominant or multifactoral trait. This form appears in a previously straight spine during the growing years.
Idiopathic scoliosis can be classified as infantile, which affects mostly male infants between birth and age 3 and causes left thoracic and right lumbar curves; juvenile, which affects both sexes between ages 4 and 10 and causes varying types of curvature; or adolescent, which generally affects girls between age 10 and achievement of skeletal maturity and causes varying types of curvature.
Source: Handbook of Diseases, 2003
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