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  2. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    The diagnosis of harlequin-type ichthyosis relies on both physical examination and laboratory tests. Physical assessment at birth is vital for the initial diagnosis of harlequin ichthyosis. Physical examination reveals characteristic symptoms of the condition, especially the abnormalities in the skin surface of newborns.

  3. Eclabium - Wikipedia

    en.wikipedia.org/wiki/Eclabium

    Eclabium can be a lifelong disorder, but drug treatment for the causing disease would heal the lips as well. For example for harlequin ichthyosis drugs such as Tazarotene [citation needed] and isotretinoin [citation needed] have been used to help the skin heal and loosen up which helps the eclabium heal. But sometimes surgery might become ...

  4. Ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Ichthyosis

    Ichthyosis comes from Greek ἰχθύς (ichthys) 'fish', since dry, scaly skin is the defining feature of all forms of ichthyosis. [ 4 ] The severity of symptoms can vary enormously, from the mildest, most common, types such as ichthyosis vulgaris , which may be mistaken for normal dry skin, up to life-threatening conditions such as harlequin ...

  5. Congenital ichthyosiform erythroderma - Wikipedia

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

    Congenital ichthyosiform erythroderma is an autosomal recessive genetic disorder. This means a child must inherit a defective pair of genes (one from each parent) to show the symptoms.

  6. Ectropion - Wikipedia

    en.wikipedia.org/wiki/Ectropion

    Cycatricial ectropion – closed eyes. Ectropion is a medical condition in which the lower eyelid turns outwards. [1] It is one of the notable aspects of newborns exhibiting congenital harlequin-type ichthyosis, but ectropion can occur due to any weakening of tissue of the lower eyelid.

  7. CHIME syndrome - Wikipedia

    en.wikipedia.org/wiki/CHIME_syndrome

    CHIME syndrome, also known as Zunich–Kaye syndrome or Zunich neuroectodermal syndrome, is a rare congenital ichthyosis first described in 1983. [1] The acronym CHIME is based on its main symptoms: colobomas, heart defects, ichthyosiform dermatosis, intellectual disability, and either ear defects or epilepsy. [2]

  8. Epidermolytic hyperkeratosis - Wikipedia

    en.wikipedia.org/wiki/Epidermolytic_hyperkeratosis

    Epidermolytic ichthyosis (EI), [a] is a severe form of dry scaly skin, that initially presents with redness, blisters, erosions, and peeling in a newborn baby. [ 5 ] [ 6 ] Hyperkeratosis typically develops several months later. [ 6 ]

  9. Ichthyosis acquisita - Wikipedia

    en.wikipedia.org/wiki/Ichthyosis_acquisita

    The development of ichthyosis in adulthood can be a manifestation of systemic disease, and it has been described in association with malignancies, drugs, endocrine and metabolic disease, HIV, infection, and autoimmune conditions. [2]: 494