Vertebral malsegmentation

Synonyms
Vertebral segmentation defect
Subtypes
Congenital fused vertebrae
Hemivertebra
Supernumerary vertebra
May Cause
Cervical spine fusion
Vertebral coronal cleft
May Be Caused by
Acrocephalosyndactyly Pfeiffer type
Acrocephalosyndactyly Saethre-Chotzen type
Aicardi syndrome
Alagille syndrome
Apert syndrome
Atelosteogenesis type 2
Berk-Tabatznik syndrome
Binder syndrome
BRESEK syndrome
Casamassima-Morton-Nance syndrome
Caudal duplication
Caudal regression syndrome
Cerebrofaciothoracic dysplasia
CHILD syndrome
Chondrodysplasia punctata
Christian spondylo-digital syndrome
Chromosome 5:del(5p) syndrome
Chromosome syndrome
Costo-vertebral segmentation defect with mesomelia
Crouzon syndrome
Currarino triad
Diabetic embryopathy
Diastematomyelia
Dobrow syndrome
Dyssegmental dysplasia
Dysspondylochondromatosis
Familial C1 posterior arch defect
Fanconi anemia
Femoral hypoplasia-unusual facies syndrome
Fetal alcohol syndrome
Goltz syndrome
Gorlin syndrome
Holoprosencephaly with caudal dysgenesis
Holt-Oram syndrome
Hypophosphatasia
Incontinentia pigmenti
Iniencephaly
Ischiospinal dysostosis
Isolated anomaly
Kabuki syndrome
Klippel-Feil syndrome
Kousseff syndrome
Larsen syndrome
LEOPARD syndrome
Lumbocostovertebral sequence
Mathieu syndrome
Meningomyelocele with spinal dysraphism
Metaphyseal-sella turcica dysplasia Rosenberg type
Multiple pterygium syndrome
Multiple synostosis syndrome
MURCS association
Noonan syndrome
Oculo-auriculo-vertebral spectrum
OEIS complex
Pfeiffer syndrome
Pfeiffer-like syndrome
PIV syndrome
Poland syndrome
Postaxial polydactyly-dental-vertebral syndrome
Robin sequence
Robinow syndrome
Saethre-Chotzen syndrome
Sakoda complex
Split notochord syndrome
Spondylocarpotarsal fusion syndrome
Spondylocostal dysostosis
Tethered cord syndrome
Trisomy 18
Trisomy 8
VATER association
VECS syndrome
Wildervanck syndrome
Vertebral segmentation defect
Acrocephalosyndactyly Pfeiffer type
Acrocephalosyndactyly Saethre-Chotzen type
Aicardi syndrome
Alagille syndrome
Apert syndrome
Atelosteogenesis type 2
Berk-Tabatznik syndrome
Binder syndrome
BRESEK syndrome
Casamassima-Morton-Nance syndrome
Caudal duplication
Caudal regression syndrome
Cerebrofaciothoracic dysplasia
CHILD syndrome
Chondrodysplasia punctata
Christian spondylo-digital syndrome
Chromosome 5:del(5p) syndrome
Chromosome syndrome
Costo-vertebral segmentation defect with mesomelia
Crouzon syndrome
Currarino triad
Diabetic embryopathy
Diastematomyelia
Dobrow syndrome
Dyssegmental dysplasia
Dysspondylochondromatosis
Familial C1 posterior arch defect
Fanconi anemia
Femoral hypoplasia-unusual facies syndrome
Fetal alcohol syndrome
Goltz syndrome
Gorlin syndrome
Holoprosencephaly with caudal dysgenesis
Holt-Oram syndrome
Hypophosphatasia
Incontinentia pigmenti
Iniencephaly
Ischiospinal dysostosis
Isolated anomaly
Kabuki syndrome
Klippel-Feil syndrome
Kousseff syndrome
Larsen syndrome
LEOPARD syndrome
Lumbocostovertebral sequence
Mathieu syndrome
Meningomyelocele with spinal dysraphism
Metaphyseal-sella turcica dysplasia Rosenberg type
Multiple pterygium syndrome
Multiple synostosis syndrome
MURCS association
Noonan syndrome
Oculo-auriculo-vertebral spectrum
OEIS complex
Pfeiffer syndrome
Pfeiffer-like syndrome
PIV syndrome
Poland syndrome
Postaxial polydactyly-dental-vertebral syndrome
Robin sequence
Robinow syndrome
Saethre-Chotzen syndrome
Sakoda complex
Split notochord syndrome
Spondylocarpotarsal fusion syndrome
Spondylocostal dysostosis
Tethered cord syndrome
Trisomy 18
Trisomy 8
VATER association
VECS syndrome
Wildervanck syndrome