Netherton's team
Netherton syndrome (NETH) - a rare genetic disorder of the dermatitis manifested by primary immunodeficiency. The disease is inherited autosomally recessively and is more common in girls.
The Netherton syndrome is caused by mutations in the SPINK5 gene encoding the LEKT1 serine protease inhibitor. The phenotypic characteristics of patients with this syndrome are: trichorrhexis invaginata (abnormal hair, described as "bamboo stalk"), early erythroderma with epidermal exfoliation, and later ichtyosis linearis circumflexa and atopy (allergies) , asthma, enterocolitis with enterocolitis atrophy). Infants show little resemblance to suck and grow poorly.
Pathological disorders:
The band was described for the first time in 1958 by Netherton.
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