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Results 1 - 9 of 9 for erythroderma OR Sezary syndrome OR psoriasis
  1. Sézary syndrome 
    Sézary syndrome is an aggressive form of a type of blood cancer called cutaneous T-cell lymphoma. Cutaneous ... skin, causing different types of skin lesions. In Sézary syndrome, the cancerous T cells, called Sézary cells, are ...
    https://medlineplus.gov/genetics/condition/sezary-syndrome - Genetics
  2. Mycosis fungoides 
    ... Campbell JJ, Clark RA, Watanabe R, Kupper TS. Sezary syndrome and mycosis fungoides arise from distinct T-cell ... JE, Jaffe ES, Wilson WH. Mycosis fungoides and Sezary syndrome. Lancet. 2008 Mar 15;371(9616):945-57. ...
    https://medlineplus.gov/genetics/condition/mycosis-fungoides - Genetics
  3. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects 
    ... male with CHILD syndrome has been reported. CHILD syndrome Ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of ...
    https://medlineplus.gov/...hthyosiform-erythroderma-and-limb-defects - Genetics
  4. Netherton syndrome 
    ... of the condition. Bamboo hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ...
    https://medlineplus.gov/genetics/condition/netherton-syndrome - Genetics
  5. Chanarin-Dorfman syndrome 
    Chanarin-Dorfman syndrome is a condition in which fats (lipids) are stored abnormally in the body. Affected individuals cannot break down certain fats called triglycerides, ...
    https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome - Genetics
  6. Keratitis-ichthyosis-deafness syndrome 
    ... is also caused by GJB2 gene mutations. Ichthyosiform erythroderma, corneal involvement, and deafness Keratitis, ichthyosis, and deafness KID syndrome Genetic Testing Registry: Autosomal recessive keratitis-ichthyosis-deafness ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  7. NSDHL gene 
    ... been found to cause congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). Most of these mutations change single protein building ...
    https://medlineplus.gov/genetics/gene/nsdhl - Genetics
  8. Vohwinkel syndrome 
    ... may also be mild reddening of the skin (erythroderma). Some affected infants are born with a tight, clear sheath covering their skin called a collodion membrane. This membrane is usually shed during the first few weeks of life. Vohwinkel syndrome is a rare disorder; about 50 cases have ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
  9. Omenn syndrome 
    ... people.In addition to immunodeficiency, children with Omenn syndrome develop autoimmunity, in which the immune system attacks the body's own tissues and organs. This abnormal immune reaction can cause very red skin (erythroderma), hair loss (alopecia), and an enlarged liver and ...
    https://medlineplus.gov/genetics/condition/omenn-syndrome - Genetics