Platyspondyly

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 ]

Subtypes
Platyspondyly with amelogenesis imperfecta
May Cause
Wide intervertebral disk space
May Be Caused by
Achondrogenesis
Achondroplasia
Anemia
Aspartylglucosaminuria
Atelosteogenesis
Atelosteogenesis type 1
Atelosteogenesis type 2
Bisphosphonate therapy
Brachyolmia
Brachyolmia-like dysplasia with amelogenesis imperfecta
Cephaloskeletal dysplasia
Chondrodysplasia-microphthalmia
Cushing syndrome
Dappled dysplasia
Deferoxamine-induced skeletal dysplasia
Dental-skeletal syndrome
Diastrophic dysplasia
Distal arthrogryposis type 2A
Dyggve-Melchior-Clausen dysplasia
Dysosteosclerosis
Ehlers-Danlos syndrome
Enchondromatosis
Fibrochondrogenesis
Fucosidosis
Gaucher disease
Gerodermia osteodysplastica
Gilles de la Tourette syndrome
GM1 gangliosidosis
Hallermann-Streiff syndrome
Homocystinuria
Hydrops - ectopic calcification - moth-eaten skeletal dysplasia
Hyperphosphatasia
Hypertrichotic osteochondrodysplasia
Hypochondrogenesis
Hypochondroplasia
Hypophosphatasia
Hypopituitarism
Hypothyroidism
Idiopathic juvenile osteoporosis
Infantile hypothyroidism
Juvenile hypothyroidism
Kniest dysplasia
Kyphomelic dysplasia
Langerhans cell histiocytosis
Larsen syndrome
Lethal osteosclerotic skeletal dysplasia
Lethal osteosclerotic skeletal dysplasia Astley-Kendall type
Lethal skeletal dysplasia-CNS degeneration
Marshall syndrome
Metaphyseal chondrodysplasia anadysplasia type
Metaphyseal chondrodysplasia Schmid type
Metaphyseal-sella turcica dysplasia Rosenberg type
Metatropic dysplasia
Morquio syndrome
Mucopolysaccharidosis type 4A
Multiple epiphyseal dysplasia
Opsismodysplasia
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteoporosis-pseudoglioma syndrome
Otospondylomegaepiphyseal dysplasia
Parastremmatic dysplasia
Patterson syndrome
Patterson-Lowry rhizomelic dysplasia
Progressive pseudorheumatoid chondrodysplasia
Pseudoachondroplasia
Pseudodiastrophic dysplasia
Pyle dysplasia
Rhizomelic bone dysplasia with retinitis pigmentosa
Rothmund-Thomson syndrome
Schwartz-Jampel syndrome
Severe combined immune deficiency
Severe hypophosphatasia
Sharony dysplasia
Short rib-polydactyly syndrome type 1
Sickle cell disease
Smith-McCort syndrome
Sotos syndrome
SPONASTRIME dysplasia
Spondylo-ocular syndrome
Spondyloenchondromatosis
Spondyloepimetaphyseal dysplasia
Spondyloepimetaphyseal dysplasia Iraqi type
Spondyloepimetaphyseal dysplasia leptodactylic type
Spondyloepimetaphyseal dysplasia short limb-hand-abnormal calcification type
Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia tarda
Spondylometaphyseal dysplasia
Spondylometaphyseal dysplasia corner-fracture type
Spondylometaphyseal dysplasia Kozlowski type
Spondylometaphyseal dysplasia Sedaghatian type
Spondyloperipheral dysplasia
Tattoo dysplasia
Thalassemia
Thanatophoric dysplasia
Thanatophoric dysplasia variant
Wolcott-Rallison syndrome
Achondrogenesis
Achondroplasia
Anemia
Aspartylglucosaminuria
Atelosteogenesis
Atelosteogenesis type 1
Atelosteogenesis type 2
Bisphosphonate therapy
Brachyolmia
Brachyolmia-like dysplasia with amelogenesis imperfecta
Cephaloskeletal dysplasia
Chondrodysplasia-microphthalmia
Cushing syndrome
Dappled dysplasia
Deferoxamine-induced skeletal dysplasia
Dental-skeletal syndrome
Diastrophic dysplasia
Distal arthrogryposis type 2A
Dyggve-Melchior-Clausen dysplasia
Dysosteosclerosis
Ehlers-Danlos syndrome
Enchondromatosis
Fibrochondrogenesis
Fucosidosis
Gaucher disease
Gerodermia osteodysplastica
Gilles de la Tourette syndrome
GM1 gangliosidosis
Hallermann-Streiff syndrome
Homocystinuria
Hydrops - ectopic calcification - moth-eaten skeletal dysplasia
Hyperphosphatasia
Hypertrichotic osteochondrodysplasia
Hypochondrogenesis
Hypochondroplasia
Hypophosphatasia
Hypopituitarism
Hypothyroidism
Idiopathic juvenile osteoporosis
Infantile hypothyroidism
Juvenile hypothyroidism
Kniest dysplasia
Kyphomelic dysplasia
Langerhans cell histiocytosis
Larsen syndrome
Lethal osteosclerotic skeletal dysplasia
Lethal osteosclerotic skeletal dysplasia Astley-Kendall type
Lethal skeletal dysplasia-CNS degeneration
Marshall syndrome
Metaphyseal chondrodysplasia anadysplasia type
Metaphyseal chondrodysplasia Schmid type
Metaphyseal-sella turcica dysplasia Rosenberg type
Metatropic dysplasia
Morquio syndrome
Mucopolysaccharidosis type 4A
Multiple epiphyseal dysplasia
Opsismodysplasia
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteoporosis-pseudoglioma syndrome
Otospondylomegaepiphyseal dysplasia
Parastremmatic dysplasia
Patterson syndrome
Patterson-Lowry rhizomelic dysplasia
Progressive pseudorheumatoid chondrodysplasia
Pseudoachondroplasia
Pseudodiastrophic dysplasia
Pyle dysplasia
Rhizomelic bone dysplasia with retinitis pigmentosa
Rothmund-Thomson syndrome
Schwartz-Jampel syndrome
Severe combined immune deficiency
Severe hypophosphatasia
Sharony dysplasia
Short rib-polydactyly syndrome type 1
Sickle cell disease
Smith-McCort syndrome
Sotos syndrome
SPONASTRIME dysplasia
Spondylo-ocular syndrome
Spondyloenchondromatosis
Spondyloepimetaphyseal dysplasia
Spondyloepimetaphyseal dysplasia Iraqi type
Spondyloepimetaphyseal dysplasia leptodactylic type
Spondyloepimetaphyseal dysplasia short limb-hand-abnormal calcification type
Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia tarda
Spondylometaphyseal dysplasia
Spondylometaphyseal dysplasia corner-fracture type
Spondylometaphyseal dysplasia Kozlowski type
Spondylometaphyseal dysplasia Sedaghatian type
Spondyloperipheral dysplasia
Tattoo dysplasia
Thalassemia
Thanatophoric dysplasia
Thanatophoric dysplasia variant
Wolcott-Rallison syndrome