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2,161 Possible Causes for Bluish-Red Border Demarcating Transition to Normal Skin, Osteogenesis Imperfecta

  • Orthostatic Syncope

    IMPERFECTA, TYPE IV OSTEOGENESIS IMPERFECTA, TYPE IX OSTEOGENESIS IMPERFECTA, TYPE V OSTEOGENESIS IMPERFECTA, TYPE VI OSTEOGENESIS IMPERFECTA, TYPE VII OSTEOGENESIS IMPERFECTA[ghr.nlm.nih.gov] How Is Osteogenesis Imperfecta (OI) Treated? There's no cure for osteogenesis imperfecta.[kidshealth.org] Also called: Brittle bone disease, OI On this page See, Play and Learn No links available Summary Osteogenesis imperfecta (OI) is a genetic disorder in which bones fracture[medlineplus.gov]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Coxa Vara

    Abstract The purpose of this study was to determine the incidence and clinical presentation of coxa vara in 283 patients with osteogenesis imperfecta (OI).[ncbi.nlm.nih.gov] Abstract In osteogenesis imperfecta (OI) because of bone fragility, deformities in load bearing regions of the body such as femoral neck and proximal femur are expected.[online.boneandjoint.org.uk] Abstract Fractures of the proximal femur frequently occur in children with osteogenesis imperfecta or fibrous dyplasia and may lead to progressive coxa vara and a "shepherds[ncbi.nlm.nih.gov]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Osteoporosis

    Osteogenesis imperfecta (OI) is an inherited bone disorder that causes fractures due to impaired production of collagen type I.[ncbi.nlm.nih.gov] Considering the lack of other osteogenesis imperfecta (OI) symptoms and signs, the patient's illness can be classified as mild.[ncbi.nlm.nih.gov] Apart from greyish-tinged sclera, no other extraskeletal features of osteogenesis imperfecta were identified.[ncbi.nlm.nih.gov]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Osteomyelitis of the Foot

    IMPERFECTA, TYPE IV OSTEOGENESIS IMPERFECTA, TYPE IX OSTEOGENESIS IMPERFECTA, TYPE V OSTEOGENESIS IMPERFECTA, TYPE VI OSTEOGENESIS IMPERFECTA, TYPE VII OSTEOGENESIS IMPERFECTA[ghr.nlm.nih.gov] […] of Osteogenesis Imperfecta Is Osteogenesis imperfecta inherited?[genome.gov] Below are some tips developed by the Osteogenesis Imperfecta Foundation for taking care of children with osteogenesis imperfecta.[orthoinfo.aaos.org]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Connective Tissue Disease

    "Osteogenesis imperfecta". Genetics Home Reference. Retrieved 2019-11-19. Reference, Genetics Home. "Stickler syndrome". Genetics Home Reference. Retrieved 2019-11-19.[en.wikipedia.org] imperfecta (brittle bone disease) – caused by poor quality collagen, or insufficient amounts of normal collagen (primarily type I), necessary for healthy, strong bones and[en.wikipedia.org] […] causes progressive deterioration of collagens, with different EDS types affecting different sites in the body, such as joints, heart valves, organ walls, arterial walls.[3] Osteogenesis[en.wikipedia.org]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Onychia

    IMPERFECTA, TYPE IV OSTEOGENESIS IMPERFECTA, TYPE IX OSTEOGENESIS IMPERFECTA, TYPE V OSTEOGENESIS IMPERFECTA, TYPE VI OSTEOGENESIS IMPERFECTA, TYPE VII OSTEOGENESIS IMPERFECTA[ghr.nlm.nih.gov] How Is Osteogenesis Imperfecta (OI) Treated? There's no cure for osteogenesis imperfecta.[kidshealth.org] Other Forms of Osteogenesis Imperfecta SERPINFI (Type VI) Patients with this form of osteogenesis imperfecta generally have moderate severity disease.[emedicine.medscape.com]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Hyperuricemia

    Keywords Gout Osteogenesis Imperfecta Hyperuricemia Osteogenesis Imperfecta Type Japanese Family These keywords were added by machine and not by the authors.[doi.org] Autosomal dominant osteogenesis imperfecta (OI) is caused by mutations in COL1A1 or COL1A2.[ncbi.nlm.nih.gov] Hyperuricemia cosegregating with osteogenesis imperfecta has been shown to be associated with a mutation in GPATCH8 using exome sequencingA ketogenic diet impairs the ability[en.wikipedia.org]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Skeletal Dysplasia

    Osteogenesis imperfecta (OI) is a heterogeneous group of disorders characterized by fragile bones.[ncbi.nlm.nih.gov] IMPERFECTA, TYPE I; OI1 166210 OSTEOGENESIS IMPERFECTA, TYPE II; OI2 166220 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 259420 OSTEOGENESIS IMPERFECTA, TYPE III; OI3 Molecular[ncbi.nlm.nih.gov] Osteogenesis imperfecta is characterized by low bone mineral density and fragile bone.[ncbi.nlm.nih.gov]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Cleidocranial Dysplasia

    imperfecta, hypophosphatasia, hypothyroidism, progeeria and Yunis-Varon syndrome.[mirc.luriechildrens.org] Other conditions that can produce similar symptoms include mandibuloacral dysplasia, pyknodysostosis, osteogenesis imperfecta, and Hajdu-Cheney syndrome.Treatment includes[en.wikipedia.org] […] seen with osteopetrosis, Paget disease and with Thorotrast administration Wormian bones can bee seen with hypothyroidism, Down Syndrome, cretinism, pyknodysostosis, and osteogenesis[learningradiology.com]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin
  • Spinal Osteochondrosis

    IMPERFECTA, TYPE IV OSTEOGENESIS IMPERFECTA, TYPE IX OSTEOGENESIS IMPERFECTA, TYPE V OSTEOGENESIS IMPERFECTA, TYPE VI OSTEOGENESIS IMPERFECTA, TYPE VII OSTEOGENESIS IMPERFECTA[ghr.nlm.nih.gov] […] of Osteogenesis Imperfecta Is Osteogenesis imperfecta inherited?[genome.gov] Below are some tips developed by the Osteogenesis Imperfecta Foundation for taking care of children with osteogenesis imperfecta.[orthoinfo.aaos.org]

    Missing: Bluish-Red Border Demarcating Transition to Normal Skin

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