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  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. 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. 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.

  5. Alkaline phosphatase, placental type - Wikipedia

    en.wikipedia.org/wiki/Alkaline_phosphatase...

    Alkaline phosphatase, placental type is a membrane-bound glycosylated dimeric enzyme, also referred to as the heat-stable form, that is expressed primarily in the placenta, although it is closely related to the intestinal form of the enzyme as well as to the placental-like form.

  6. Placental disease - Wikipedia

    en.wikipedia.org/wiki/Placental_disease

    A placental disease is any disease, disorder, or pathology of the placenta. [ 1 ] [ 2 ] Ischemic placental disease leads to the attachment of the placenta to the uterine wall to become under-perfused, causing uteroplacental ischemia.

  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. Disease starts on your plate, cardiologist says — here's what ...

    www.aol.com/disease-starts-plate-cardiologist...

    Dr. Aseem Malhotra, a cardiologist and public health campaigner based in London, says Americans' foods are fueling chronic diseases. He shares his warnings and tips with Fox News Digital.

  9. Sulfatidosis - Wikipedia

    en.wikipedia.org/wiki/Sulfatidosis

    Metachromatic leukodystrophy and multiple sulfatase deficiency are classified as sulfatidoses. [2] [3] Treatment. This section is empty. You can help by adding to it.