When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. 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.

  3. Steroid sulfatase - Wikipedia

    en.wikipedia.org/wiki/Steroid_sulfatase

    A congenital deficiency in the enzyme is associated with X-linked ichthyosis, a scaly-skin disease affecting roughly 1 in every 2,000 to 6,000 males. [7] [8] The excessive skin scaling and hyperkeratosis is caused by a lack of breakdown and thus accumulation of cholesterol sulfate, a steroid that stabilizes cell membranes and adds cohesion, in the outer layers of the skin.

  4. Multiple sulfatase deficiency - Wikipedia

    en.wikipedia.org/wiki/Multiple_sulfatase_deficiency

    Multiple sulfatase deficiency (MSD), also known as Austin disease, [1] or mucosulfatidosis, [1] is a very rare autosomal recessive [2] lysosomal storage disease [3] caused by a deficiency in multiple sulfatase enzymes, or in formylglycine-generating enzyme, which activates sulfatases. [4]: 502 [5] It is similar to mucopolysaccharidosis. [6]

  5. X-linked recessive inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_recessive_inheritance

    X-linked ichthyosis, a form of ichthyosis caused by a hereditary deficiency of the steroid sulfatase (STS) enzyme. It is fairly rare, affecting one in 2,000 to one in 6,000 males. [12] X-linked agammaglobulinemia (XLA), which affects the body's ability to fight infection. XLA patients do not generate mature B cells. [13]

  6. Hunter syndrome - Wikipedia

    en.wikipedia.org/wiki/Hunter_syndrome

    Hunter syndrome is caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). [2] [3] The lack of this enzyme causes heparan sulfate and dermatan sulfate to accumulate in all body tissues. [4] Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. [4] The symptoms of Hunter syndrome are comparable ...

  7. Mucopolysaccharidosis - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis

    MPS II, Hunter syndrome or iduronate sulfatase deficiency, is caused by lack of the enzyme iduronate sulfatase. Hunter syndrome has two clinical subtypes and (since it shows X-linked recessive inheritance) is the only one of the mucopolysaccharidoses in which the mother alone can pass the defective gene to a son.

  8. The symptoms of influenza A and B can be identical, experts ...

    www.aol.com/news/symptoms-influenza-b-identical...

    Whether you have influenza A or B, you can expect to develop the same general set of symptoms, the experts say. In fact, experts sometimes use the term "flu-like illness" to refer to other ...

  9. Steroid sulfatase deficiency - Wikipedia

    en.wikipedia.org/?title=Steroid_sulfatase...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Steroid_sulfatase_deficiency&oldid=310598357"https://en.wikipedia.org/w/index.php?title=Steroid_sulfatase