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  2. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    The skin was dry and hard and seemed to be cracked in many places, somewhat resembling the scales of a fish. The mouth was large and round and open. It had no external nose, but two holes where the nose should have been.

  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. 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]

  5. These Pictures Will Help You Identify the Most Common Skin Rashes

    www.aol.com/pictures-help-identify-most-common...

    OTC skin protectants like zinc acetate, zinc carbonate, zinc oxide, and calamine can also help dry the oozing and weeping, while baking soda or colloidal oatmeal may help with the itch, the FDA ...

  6. These Pictures Will Help You Figure Out What That Weird Rash ...

    www.aol.com/pictures-help-figure-weird-rash...

    26 pictures of skin rashes to help you identify your skin rash. Plus, doctor-approved at-home skin rash remedies and when to see a doctor for your skin rash. ... Eczema causes dry, rough, flaky ...

  7. X-linked ichthyosis - Wikipedia

    en.wikipedia.org/wiki/X-linked_ichthyosis

    X-linked ichthyosis (abbreviated XLI) is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000 to 1 in 6000 males. [2] XLI manifests with dry, scaly skin [3] and is due to deletions [4] [5] or mutations [6] in the STS gene.