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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. 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 ...

  4. Sclera - Wikipedia

    en.wikipedia.org/wiki/Sclera

    The sclera is opaque due to the irregularity of the Type I [10] collagen fibers, as opposed to the near-uniform thickness and parallel arrangement of the corneal collagen. Moreover, the cornea bears more mucopolysaccharide (a carbohydrate that has among its repeating units a nitrogenous sugar, hexosamine) to embed the fibrils.

  5. Malan syndrome - Wikipedia

    en.wikipedia.org/wiki/Malan_syndrome

    Malan syndrome is defined by initial overgrowth and mild-to-severe intellectual disability.Almost all individuals with Malan syndrome display above-average height, weight, and head circumference in early life, but only one-third of adults with Malan syndrome are >2 standard deviations above the mean.

  6. Pseudoxanthoma elasticum - Wikipedia

    en.wikipedia.org/wiki/Pseudoxanthoma_elasticum

    Pseudoxanthoma elasticum (PXE) is a genetic disease that causes mineralization of elastic fibers in some tissues. The most common problems arise in the skin and eyes, and later in blood vessels in the form of premature atherosclerosis.

  7. LMNA-related congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/LMNA-related_congenital...

    Lamin A/C congenital muscular dystrophy (CMD) (L-CMD, congenital muscular dystrophy associated to the LMNA gene or Emery-Dreifuss muscular dystrophy II) is a disease that it is included in laminopathies.

  8. Dentinogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Dentinogenesis_imperfecta

    Discoloured teeth - teeth may be amber, brown, blue or opalescent Bulbous shape to the tooth crown due to cervical constriction Tooth wear /Non-carious tooth surface loss (NCTSL) - due to the poorly mineralised dentine, the enamel of the tooth is unsupported and subsequently shears or chips off as it is subjected to biting forces.

  9. Chronic relapsing inflammatory optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Chronic_relapsing...

    Chronic relapsing inflammatory optic neuropathy (CRION) is a form of recurrent optic neuritis that is steroid responsive and dependent. [1] Patients typically present with pain associated with visual loss. [1] CRION is a clinical diagnosis of exclusion, and other demyelinating, autoimmune, and systemic causes should be ruled out. [3]

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