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  2. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    Hunter Steinitz (born October 17, 1994, 29 years old) is one of only twelve Americans living with the disease and is profiled on the National Geographic "Extraordinary Humans: Skin" special. Mui Thomas (born in 1992 in Hong Kong, 31 years old) qualified as the first rugby referee with harlequin ichthyosis.

  3. Lamellar ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Lamellar_ichthyosis

    Most cases (approximately 75%) of collodion baby will go on to develop a type of autosomal recessive congenital ichthyosis (either lamellar ichthyosis or congenital ichthyosiform erythroderma ). [5] In around 10% of cases the baby sheds this layer of skin and has normal skin for the rest of its life. [2] [5] This is known as self-healing ...

  4. Harlequin color change - Wikipedia

    en.wikipedia.org/wiki/Harlequin_color_change

    Harlequin color change is a cutaneous condition seen in newborn babies characterized by momentary red color changes of half the child, sharply demarcated at the body's midline. This transient change occurs in approximately 10% of healthy newborns. [1] It is seen usually between two and five days of birth. The condition lasts from 30 seconds to ...

  5. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye ), a white forelock or patches of light skin. These basic features constitute type 2 of the condition; in type 1, there ...

  6. Epidermolysis bullosa - Wikipedia

    en.wikipedia.org/wiki/Epidermolysis_bullosa

    Epidermolysis bullosa ( EB) is a group of rare medical conditions that result in easy blistering of the skin and mucous membranes. Blisters occur with minor trauma or friction and are painful. Its severity can range from mild to fatal. [7] Inherited EB is a rare disease with a prevalence in the United States of 8.2 per million live births. [8]

  7. Cat eye syndrome - Wikipedia

    en.wikipedia.org/wiki/Cat_eye_syndrome

    Cat-eye syndrome (CES) or Schmid–Fraccaro syndrome is a rare condition caused by an abnormal extra chromosome, i.e. a small supernumerary marker chromosome. [2] This chromosome consists of the entire short arm and a small section of the long arm of chromosome 22. In consequence, individuals with the cat-eye syndrome have three ( trisomic) or ...

  8. Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/Ehlers–Danlos_syndrome

    The skin may tear and bruise easily, and may heal with abnormal atrophic scars; atrophic scars that look like cigarette paper are a sign seen including in those whose skin might appear otherwise normal. In some subtypes, though not the hypermobile subtype, redundant skin folds occur, especially on the eyelids. Redundant skin folds are areas of ...

  9. Boa constrictor gives birth to 14 baby snakes after living ...

    www.aol.com/news/boa-constrictor-gives-birth-14...

    July 2, 2024 at 6:28 PM. Ronaldo, a 6-foot Brazilian rainbow boa constrictor kept at a school in England, was thought to be male — until the snake gave birth to 14 babies last month. The boa had ...

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