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  2. Osteogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Osteogenesis_imperfecta

    The homozygous mutation causes prenatal onset of recurrent fractures of the ribs and long bones, demineralization, decreased ossification of the skull, and blue sclerae; it is clinically type II or type III. [77] Family members who are heterozygous for OI XVI may have recurrent fractures, osteopenia and blue sclerae. [77] [78]

  3. Osteochondrodysplasia - Wikipedia

    en.wikipedia.org/wiki/Osteochondrodysplasia

    In classic non-deforming osteogenesis imperfecta with blue sclerae or common variable osteogenesis imperfecta with normal sclerae, nearly 60% of cases are de novo. COL1A1/2-related osteogenesis imperfecta is identified by repeated fractures with trivial trauma, defective dentinogenesis imperfecta (DI), and hearing loss.

  4. Daentl Townsend Siegel syndrome - Wikipedia

    en.wikipedia.org/wiki/Daentl_Townsend_Siegel...

    Daentl Townsend Siegel syndrome is a very rare disorder characterized by blue sclerae, kidney malfunction, thin skin, and hydrocephalus. It was first identified by D.L. Daentl et al. in 1978. [ 1 ] Daentl Townsend Siegel syndrome is also known as "Hydrocephalus blue sclera nephropathy" and "Familial nephrosis, hydrocephalus, thin skin, blue ...

  5. Dentinogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Dentinogenesis_imperfecta

    Rootless molars [2] [This is not a comprehensive list] It can be useful to enquire about symptoms of osteogenesis imperfecta, as Type I Dentinogenesis Imperfecta (Shield's Classification) is associated with osteogenesis imperfecta. [2] Notable information includes: History of bone fracture caused by minimal trauma; Short stature; Blue sclera

  6. Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/Ehlers–Danlos_syndrome

    Brittle-cornea syndrome is characterized by the progressive thinning of the cornea, early-onset progressive keratoglobus or keratoconus, nearsightedness, hearing loss, and blue sclerae. [ 5 ] [ 36 ] Classic symptoms, such as hypermobile joints and hyperelastic skin, are also seen often. [ 37 ]

  7. Kabuki syndrome - Wikipedia

    en.wikipedia.org/wiki/Kabuki_syndrome

    Child displaying typical facial phenotype of Kabuki syndrome. Specific symptoms for Kabuki syndrome vary, with large differences between affected individuals. [3] Most people with Kabuki syndrome have distinctive facial features that include arched eyebrows, long eyelashes, elongated eyelids with lower lids that turn out, prominent ears, a flat tip of the nose and a downward slant to the mouth.

  8. Intraocular hemorrhage - Wikipedia

    en.wikipedia.org/wiki/Intraocular_hemorrhage

    Intraocular hemorrhage is classified based on the location of the bleeding: Hyphema (in the anterior chamber); Suprachoroidal hemorrhage (SCH) is a rare complication of intraocular surgery in which blood from the ciliary arteries enters the space between the choroid and the sclera.

  9. Chronic multifocal Langerhans cell histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Chronic_multifocal_Langer...

    The diagnosis may be suspected based on symptoms and MRI and confirmed by tissue biopsy. [6] [7] Blood tests may show anaemia, and less commonly a low white blood cell count and low platelet count. [5] Treatment may involve surgery, chemotherapy, radiation therapy, and certain medicines. [7]