Overview
Osteodystrophy is a general term for a dystrophic growth of the bone.
One form is renal osteodystrophy.
| Congenital malformations and deformations of musculoskeletal system (Q65-Q79, 754-756) |
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| Limbs | hip: Dislocation of hip/Hip dysplasia - Upington disease
feet (Club foot, Flat feet, Pes cavus)
systemic dislocations Larsen syndrome
head, face, spine and chest: skull, face and jaw (Dolichocephaly, Greig cephalopolysyndactyly syndrome, Plagiocephaly) - spine Scoliosis - chest (Pectus excavatum, Pectus carinatum)
any combination head, face, jaw, upper limb, lower limb, pelvis, dactyly Antley-Bixler syndrome - Schmitt Gillenwater Kelly syndrome
dactyly Polydactyly/Syndactyly (Webbed toes) - Cenani Lenz syndactylism
reduction deficits (Acheiropodia, Amelia, Ectrodactyly, Phocomelia)
upper limb (Cleidocranial dysostosis, Madelung's deformity, Sprengel's deformity, Wallis Zieff Goldblatt syndrome)
knee (Genu valgum, Genu varum)
other Arthrogryposis |
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| Skull and facial bones | Carpenter syndrome - Craniodiaphyseal dysplasia - Craniosynostosis (Scaphocephaly) - Crouzon syndrome - Hypertelorism - Macrocephaly - Oxycephaly - Platybasia - Saethre-Chotzen syndrome - Treacher Collins syndrome - Trigonocephaly |
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| Spine and bony thorax | Klippel-Feil syndrome - Spondylolisthesis - Cervical rib - Bifid rib |
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| Osteochondrodysplasia | developement of cartilage, tubular bones and spine: Achondrogenesis/Hypochondrogenesis - Boomerang dysplasia - Thanatophoric dysplasia - Short rib-polydactyly syndrome - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome), Achondroplasia (Hypochondroplasia, Osteosclerosis congenita) - Ellis-van Creveld syndrome - Otospondylomegaepiphyseal dysplasia - Spondyloepiphyseal dysplasia congenita
- Osteogenesis imperfecta - McCune-Albright syndrome - Osteopetrosis - Metaphyseal dysplasia - Recessive multiple epiphyseal dysplasia - Hereditary multiple exostoses - Osteopoikilosis - Chondrodystrophy - Osteodystrophy - Atelosteogenesis, type II - Diastrophic dysplasia |
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| Other | abdominal wall (Congenital diaphragmatic hernia, Omphalocele, Gastroschisis, Prune belly syndrome) - Ehlers-Danlos syndrome |
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| See also non-congenital conditions (M, 710-739) |
