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Results 1 - 10 of 53 for Cartilage development disorder
  1. Atelosteogenesis type 2 
    Atelosteogenesis type 2 is a severe disorder of cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. This disorder is ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-2 - Genetics
  2. Diastrophic dysplasia 
    Diastrophic dysplasia is a disorder of cartilage and bone development. Affected individuals have short stature with very short arms and legs. Most also have early-onset joint pain (osteoarthritis) and ...
    https://medlineplus.gov/genetics/condition/diastrophic-dysplasia - Genetics
  3. X-linked chondrodysplasia punctata 1 
    X-linked chondrodysplasia punctata 1 is a disorder of cartilage and bone development that occurs almost exclusively in males. Chondrodysplasia punctata is an abnormality that appears on x-rays as spots (stippling) near the ends of ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-1 - Genetics
  4. Multiple epiphyseal dysplasia 
    Multiple epiphyseal dysplasia is a disorder of cartilage and bone development primarily affecting the ends of the long bones in the arms and legs (epiphyses). There are two types of multiple epiphyseal ...
    https://medlineplus.gov/.../condition/multiple-epiphyseal-dysplasia - Genetics
  5. Achondrogenesis 
    Achondrogenesis is a group of severe disorders that affect cartilage and bone development. These conditions are characterized by a small body, short limbs, and other skeletal abnormalities. As a result of serious health problems, infants ...
    https://medlineplus.gov/genetics/condition/achondrogenesis - Genetics
  6. Camurati-Engelmann disease 
    ... regulate the formation and growth of bone and cartilage, a tough, flexible ... Camurati-Engelmann disease result in the production of an overly active ...
    https://medlineplus.gov/.../condition/camurati-engelmann-disease - Genetics
  7. Legg-Calvé-Perthes disease 
    ... is later converted to bone, except for the cartilage that continues to cover and protect ... disease lead to production of an altered protein; collagen ...
    https://medlineplus.gov/.../condition/legg-calve-perthes-disease - Genetics
  8. Spondyloperipheral dysplasia 
    ... molecules, the abnormal COL2A1 protein builds up in cartilage cells (chondrocytes). These changes disrupt the normal development of bones and ... ulna Genetic Testing ...
    https://medlineplus.gov/.../condition/spondyloperipheral-dysplasia - Genetics
  9. Platyspondylic lethal skeletal dysplasia, Torrance type 
    ... molecules, the abnormal COL2A1 protein builds up in cartilage cells (chondrocytes). These changes disrupt the ... Platyspondylic chondrodysplasia, Torrance-Luton type Platyspondylic skeletal dysplasia, ...
    https://medlineplus.gov/...c-lethal-skeletal-dysplasia-torrance-type - Genetics
  10. Familial osteochondritis dissecans 
    ... of familial osteochondritis dissecans include short stature and development of a joint disorder called osteoarthritis at an early age. Osteoarthritis is characterized by the breakdown of joint cartilage and the underlying bone. It causes pain and ...
    https://medlineplus.gov/.../familial-osteochondritis-dissecans - Genetics
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