Bowed tubular bones

Achondroplasia is a genetic disorder whose primary feature is dwarfism. In those with the condition, the arms and legs are short, while the torso is typically of normal length. [Source: Wikipedia ]

May Cause
Cortical bone thickening
May Be Caused by
Achondroplasia
Antley-Bixler syndrome
Atelosteogenesis
Atelosteogenesis type 2
Blomstrand dysplasia
Blount disease
Boomerang dysplasia
Brachmann-de Lange syndrome
Campomelic dysplasia
Chondrodysplasia punctata tibial-metacarpal type
Cloverleaf skull deformity
Contractural arachnodactyly
Cumming syndrome
Diastrophic dysplasia
Distal osteosclerosis
Dyssegmental dysplasia
Ellis-van Creveld syndrome
Epidermal nevus syndrome
Familial congenital bowing of the long bones
Fibrocartilaginous dysplasia
Fibrochondrogenesis
Fibrous dysplasia
Fibular aplasia-ectrodactyly
Frank-ter Haar syndrome
Fuhrmann syndrome
GM1 gangliosidosis
Grant syndrome
Hemihypertrophy
Homocystinuria
Hydrolethalus syndrome
Hyperparathyroidism
Hyperphosphatasemia
Hypophosphatasia
Infant of diabetic mother
Infantile multisystem inflammatory disease
Intrauterine positional deformity
Isolated anomaly
Klippel-Trénaunay-Weber syndrome
Koller syndrome
Kyphomelic dysplasia
Larsen syndrome
Lethal osteosclerotic skeletal dysplasia Astley-Kendall type
Maffucci syndrome
Melnick-Needles osteodysplasty
Metaphyseal chondrodysplasia anadysplasia type
Metaphyseal chondrodysplasia Jansen type
Metaphyseal chondrodysplasia McKusick type
Metaphyseal chondrodysplasia Schmid type
Mucolipidosis
Mucopolysaccharidosis
Neurofibromatosis
Occipital horn syndrome
Oligohydramnios
Ophthalmo-mandibulo-melic dysplasia
Osteogenesis imperfecta
Osteolysis with nephropathy
Osteomalacia
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachydysostosis of the fibula
Pacman dysplasia
Panostotic fibrous dysplasia
Parastremmatic dysplasia
Physiologic bowing of infancy
Pointer syndrome
Precocious osteodysplasty
Proximal femoral deficiency
Pseudoarthrosis
Pseudohypoparathyroidism
Rickets
Schwarz-Lélek syndrome
Serpentine fibula-polycystic kidney syndrome
Short rib-polydactyly syndrome
Thanatophoric dysplasia
Thanatophoric dysplasia variant
Weismann-Netter syndrome
Achondroplasia
Antley-Bixler syndrome
Atelosteogenesis
Atelosteogenesis type 2
Blomstrand dysplasia
Blount disease
Boomerang dysplasia
Brachmann-de Lange syndrome
Campomelic dysplasia
Chondrodysplasia punctata tibial-metacarpal type
Cloverleaf skull deformity
Contractural arachnodactyly
Cumming syndrome
Diastrophic dysplasia
Distal osteosclerosis
Dyssegmental dysplasia
Ellis-van Creveld syndrome
Epidermal nevus syndrome
Familial congenital bowing of the long bones
Fibrocartilaginous dysplasia
Fibrochondrogenesis
Fibrous dysplasia
Fibular aplasia-ectrodactyly
Frank-ter Haar syndrome
Fuhrmann syndrome
GM1 gangliosidosis
Grant syndrome
Hemihypertrophy
Homocystinuria
Hydrolethalus syndrome
Hyperparathyroidism
Hyperphosphatasemia
Hypophosphatasia
Infant of diabetic mother
Infantile multisystem inflammatory disease
Intrauterine positional deformity
Isolated anomaly
Klippel-Trénaunay-Weber syndrome
Koller syndrome
Kyphomelic dysplasia
Larsen syndrome
Lethal osteosclerotic skeletal dysplasia Astley-Kendall type
Maffucci syndrome
Melnick-Needles osteodysplasty
Metaphyseal chondrodysplasia anadysplasia type
Metaphyseal chondrodysplasia Jansen type
Metaphyseal chondrodysplasia McKusick type
Metaphyseal chondrodysplasia Schmid type
Mucolipidosis
Mucopolysaccharidosis
Neurofibromatosis
Occipital horn syndrome
Oligohydramnios
Ophthalmo-mandibulo-melic dysplasia
Osteogenesis imperfecta
Osteolysis with nephropathy
Osteomalacia
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachydysostosis of the fibula
Pacman dysplasia
Panostotic fibrous dysplasia
Parastremmatic dysplasia
Physiologic bowing of infancy
Pointer syndrome
Precocious osteodysplasty
Proximal femoral deficiency
Pseudoarthrosis
Pseudohypoparathyroidism
Rickets
Schwarz-Lélek syndrome
Serpentine fibula-polycystic kidney syndrome
Short rib-polydactyly syndrome
Thanatophoric dysplasia
Thanatophoric dysplasia variant
Weismann-Netter syndrome