ArticlePediatric dermatology
Hair Improvement in SPINK5-sEDD (Netherton Syndrome) With Dupilumab.
Article in Pediatric dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
6 authors.
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Abstract
SPINK5-syndromic epidermal differentiation disorder (sEDD) (formerly known as Netherton syndrome) is a rare genodermatosis characterized by ichthyosis linearis circumflexa, atopic diathesis, and trichorrhexis invaginata. We report an 11-year-old girl with SPINK5-sEDD who experienced marked improvement in hair density, texture, and pruritus following dupilumab. The early and sustained hair response suggests that IL-4/IL-13 blockade may modulate the perifollicular inflammatory environment and enhance follicular function. This observation supports emerging evidence that dupilumab may confer hair benefits in SPINK5-sEDD and underscores the need for systematic evaluation of this effect.
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