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  2. Lamellar ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Lamellar_ichthyosis

    Lamellar ichthyosis, also known as ichthyosis lamellaris and nonbullous congenital ichthyosis, is a rare inherited skin disorder, affecting around 1 in 600,000 people. Presentation [ edit ]

  3. Ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Ichthyosis

    Ichthyosis (also named fish scale disease) [1] is a family of genetic skin disorders characterized by dry, thickened, scaly skin. [2] The more than 20 types of ichthyosis range in severity of symptoms, outward appearance, underlying genetic cause and mode of inheritance (e.g., dominant, recessive , autosomal or X-linked ). [ 3 ]

  4. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    A child with Harlequin-type ichthyosis. Visible plates on the skin and changes in the appearance of the ears and fingers, are symptoms of Harlequin-type ichthyosis. [10] Newborns with harlequin-type ichthyosis present with thick, fissured armor-plate hyperkeratosis. [11] Sufferers feature severe cranial and facial deformities.

  5. Model Jeyza Gary Opens Up About the Rare Condition That ... - AOL

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  6. Ichthyosis vulgaris - Wikipedia

    en.wikipedia.org/wiki/Ichthyosis_vulgaris

    Ichthyosis vulgaris (also known as "autosomal dominant ichthyosis" [1] and "Ichthyosis simplex" [1]) is a skin disorder causing dry, scaly skin. It is the most common form, and one of the mildest forms, of ichthyosis, [2] [3]: 486 affecting around 1 in 250 people. [4] For this reason it is known as common ichthyosis.

  7. Congenital ichthyosiform erythroderma - Wikipedia

    en.wikipedia.org/wiki/Congenital_ichthyosiform...

    Eclabium (eversion of the lips), ectropion and alopecia (hair loss) are more common in congenital ichthyosiform erythroderma than in lamellar ichthyosis. [ 3 ] [ non-primary source needed ] Congenital ichthyosiform erythroderma can present very similarly to lamellar ichthyosis and they often share characteristics, though the two conditions can ...

  8. Ruzicka Goerz Anton syndrome - Wikipedia

    en.wikipedia.org/wiki/Ruzicka_Goerz_Anton_syndrome

    The patient had ichthyosis congenita as well as deafness and retarded mental development. Further studies showed several skeletal deformities including brachydactyly, clinodactyly, and extra ribs. One year earlier, the patient had developed thyroid carcinoma, but whether or not this is due to the syndrome is unknown. The patient was treated ...

  9. Man on carnivore diet has cholesterol of 1,000, sees shocking ...

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    The patient said he lost weight, had more energy and experienced improved mental clarity, according to a case report in JAMA Cardiology. But his primary care doctor noticed the fatty yellow bumps ...