SSSS often includes a widespread painful erythroderma, often involving the face, diaper, and other intertriginous areas.
2.
Children who survive the neonatal period usually evolve to a less severe phenotype, resembling a severe congenital ichthyosiform erythroderma.
3.
Increased transepidermal water loss resulting from the disturbance of corneocyte barrier function in erythroderma may cause profound metabolic abnormalities and hypernatremia, particularly in neonates.
4.
Omenn Syndrome ( OS ) is a severe "'immunodeficiency "'disease, mostly characterized by scaly "'erythroderma "'and severe reddening of the skin.
5.
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.
6.
"' 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.
7.
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.
8.
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 ."
9.
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.
10.
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.
How to say erythroderma in Hindi and what is the meaning of erythroderma in Hindi? erythroderma Hindi meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.
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