Congenital vertebral abnormality

Congenital vertebral anomalies are a collection of malformations of the spine. Most, around 85%, are not clinically significant, but they can cause compression of the spinal cord by deforming the vertebral canal or causing instability. [Source: Wikipedia ]

May Be Caused by
Achondrogenesis type 1
Achondrogenesis type 2
Achondroplasia
Acrocephalosyndactyly Pfeiffer type
Acrocephalosyndactyly Saethre-Chotzen type
Acrodysostosis
Aicardi syndrome
Alagille syndrome
Apert syndrome
Atelosteogenesis
Atelosteogenesis type 2
Binder syndrome
Brachyolmia
Campomelic dysplasia
Cauda equina syndrome
Caudal regression syndrome
CHILD syndrome
Chondrodysplasia punctata
Cleidocranial dysostosis
Cockayne syndrome
Crouzon syndrome
Currarino triad
Diastrophic dysplasia
Distal arthrogryposis type 2A
Dyggve-Melchior-Clausen dysplasia
Dysosteosclerosis
Dyssegmental dysplasia
Dysspondylochondromatosis
Ehlers-Danlos syndrome
Enchondromatosis
Fanconi anemia
Femoral hypoplasia-unusual facies syndrome
Fetal alcohol syndrome
Gerodermia osteodysplastica
GM1 gangliosidosis
Goltz syndrome
Gorlin syndrome
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
Holt-Oram syndrome
Homocystinuria
Hyperphosphatasia
Hypochondroplasia
Hypophosphatasia
Hypothyroidism
Incontinentia pigmenti
Infantile hypothyroidism
Klippel-Feil syndrome
Kniest dysplasia
Larsen syndrome
LEOPARD syndrome
Marfan syndrome
Marshall syndrome
Melnick-Needles osteodysplasty
Metaphyseal chondrodysplasia Jansen type
Metaphyseal chondrodysplasia McKusick type
Metatropic dysplasia
Morquio syndrome
Mucopolysaccharidosis
Multiple epiphyseal dysplasia
Multiple pterygium syndrome
Nail-patella syndrome
Neurofibromatosis
Noonan syndrome
Oculo-auriculo-vertebral spectrum
Oculovertebral syndrome
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteopetrosis
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Parastremmatic dysplasia
Patterson syndrome
Poland syndrome
Popliteal pterygium syndrome
Prader-Willi syndrome
Progeria
Pseudoachondroplasia
Pyle dysplasia
Robin sequence
Robinow syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Schwartz-Jampel syndrome
Seckel syndrome
Shawl scrotum syndrome
Short rib-polydactyly syndrome
Split notochord syndrome
SPONASTRIME dysplasia
Spondylocarpotarsal fusion syndrome
Spondylocostal dysostosis
Spondyloepimetaphyseal dysplasia
Spondyloepiphyseal dysplasia
Spondylometaphyseal dysplasia
Spondyloperipheral dysplasia
Stickler syndrome
Tethered cord syndrome
Thanatophoric dysplasia
Trisomy 13
Trisomy 18
Trisomy 21
VATER association
Wildervanck syndrome
Williams syndrome
Achondrogenesis type 1
Achondrogenesis type 2
Achondroplasia
Acrocephalosyndactyly Pfeiffer type
Acrocephalosyndactyly Saethre-Chotzen type
Acrodysostosis
Aicardi syndrome
Alagille syndrome
Apert syndrome
Atelosteogenesis
Atelosteogenesis type 2
Binder syndrome
Brachyolmia
Campomelic dysplasia
Cauda equina syndrome
Caudal regression syndrome
CHILD syndrome
Chondrodysplasia punctata
Cleidocranial dysostosis
Cockayne syndrome
Crouzon syndrome
Currarino triad
Diastrophic dysplasia
Distal arthrogryposis type 2A
Dyggve-Melchior-Clausen dysplasia
Dysosteosclerosis
Dyssegmental dysplasia
Dysspondylochondromatosis
Ehlers-Danlos syndrome
Enchondromatosis
Fanconi anemia
Femoral hypoplasia-unusual facies syndrome
Fetal alcohol syndrome
Gerodermia osteodysplastica
GM1 gangliosidosis
Goltz syndrome
Gorlin syndrome
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
Holt-Oram syndrome
Homocystinuria
Hyperphosphatasia
Hypochondroplasia
Hypophosphatasia
Hypothyroidism
Incontinentia pigmenti
Infantile hypothyroidism
Klippel-Feil syndrome
Kniest dysplasia
Larsen syndrome
LEOPARD syndrome
Marfan syndrome
Marshall syndrome
Melnick-Needles osteodysplasty
Metaphyseal chondrodysplasia Jansen type
Metaphyseal chondrodysplasia McKusick type
Metatropic dysplasia
Morquio syndrome
Mucopolysaccharidosis
Multiple epiphyseal dysplasia
Multiple pterygium syndrome
Nail-patella syndrome
Neurofibromatosis
Noonan syndrome
Oculo-auriculo-vertebral spectrum
Oculovertebral syndrome
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteopetrosis
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Parastremmatic dysplasia
Patterson syndrome
Poland syndrome
Popliteal pterygium syndrome
Prader-Willi syndrome
Progeria
Pseudoachondroplasia
Pyle dysplasia
Robin sequence
Robinow syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Schwartz-Jampel syndrome
Seckel syndrome
Shawl scrotum syndrome
Short rib-polydactyly syndrome
Split notochord syndrome
SPONASTRIME dysplasia
Spondylocarpotarsal fusion syndrome
Spondylocostal dysostosis
Spondyloepimetaphyseal dysplasia
Spondyloepiphyseal dysplasia
Spondylometaphyseal dysplasia
Spondyloperipheral dysplasia
Stickler syndrome
Tethered cord syndrome
Thanatophoric dysplasia
Trisomy 13
Trisomy 18
Trisomy 21
VATER association
Wildervanck syndrome
Williams syndrome