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Netherton syndrome (NS; OMIM: 256500) is a rare autosomal recessively inherited disease due to SPINK5 mutations. Hair and inflammatory skin involvement are variable along with allergies. Morbidity and mortality are… Click to show full abstract
Netherton syndrome (NS; OMIM: 256500) is a rare autosomal recessively inherited disease due to SPINK5 mutations. Hair and inflammatory skin involvement are variable along with allergies. Morbidity and mortality are high, particularly in infancy. A detailed clinical analysis of a NS patient cohort should broaden the understanding of nutritional challenges and allergic comorbidities.
Keywords:
netherton syndrome;
prevalence risk;
factors nutritional;
nutritional deficiency;
risk factors;
cohort
Journal Title: Pediatric Allergy and Immunology
Year Published: 2023
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Journal Title: Pediatric Allergy and Immunology
Year Published: 2023
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!