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erythroderma meaning in Hindi
erythroderma sentence in Hindi
Examples
More: Next- SSSS often includes a widespread painful erythroderma, often involving the face, diaper, and other intertriginous areas.
- Children who survive the neonatal period usually evolve to a less severe phenotype, resembling a severe congenital ichthyosiform erythroderma.
- Increased transepidermal water loss resulting from the disturbance of corneocyte barrier function in erythroderma may cause profound metabolic abnormalities and hypernatremia, particularly in neonates.
- Omenn Syndrome ( OS ) is a severe "'immunodeficiency "'disease, mostly characterized by scaly "'erythroderma "'and severe reddening of the skin.
- Some of the most severe and life-threatening examples of drug eruptions are erythema multiforme, Stevens Johnson syndrome, toxic epidermal necrolysis, hypersensitivity vasculitis, DRESS syndrome, erythroderma and exanthematous pustulosis.
- "' Congenital hemidysplasia with ichthyosiform erythroderma and limb defects "'( also known as " CHILD syndrome " ) is a genetic disorder with onset at birth seen almost exclusively in females.
- As affected individuals get older, blistering is less frequent, erythroderma becomes less evident, and the skin becomes thick ( hyperkeratotic ), especially over joints, on areas of skin that come into contact with each other, or on the scalp or neck.
- Some centers view the condition with an holistic approach, testing for infections, food sensitives and other conditions that may trigger disease progression, treating it first before moving to other medications . " [ A ] ntibiotic treatment for S . aureus infection leads to decreased erythroderma and tumor size without other adjunct treatment ."
- Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.
- Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.
Meaning
noun.- any skin disorder involving abnormal redness