2021
DOI: 10.1111/pde.14523
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Treatment practices in the management of scabies in infants younger than two months

Abstract: Scabies is an ectoparasitic disease affecting more than 200 million people worldwide. 1 Although scabies affects all ages, children and infants carry a particularly high burden of disease. Prevalence in children is 5%-10% in some tropical resource-limited countries and as high as 34.1% in infants less than 1 year in the Solomon Islands. 1,2 Bacterial superinfection of scabies lesions can lead to systemic sequelae, including acute post-streptococcal glomerulonephritis and acute rheumatic fever. 1 Therefore, tr… Show more

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Cited by 10 publications
(9 citation statements)
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“…10,12 Burning sensation, irritant contact dermatitis, and erythema are the other side effects. 7,9,10,14,16 Midfacial edema has also been reported. 14 Compatibly, 76% of our cohort had no side effects or suffered mild skin dryness, which was well tolerated.…”
Section: Discussionmentioning
confidence: 97%
“…10,12 Burning sensation, irritant contact dermatitis, and erythema are the other side effects. 7,9,10,14,16 Midfacial edema has also been reported. 14 Compatibly, 76% of our cohort had no side effects or suffered mild skin dryness, which was well tolerated.…”
Section: Discussionmentioning
confidence: 97%
“…It is caused by pathogenic variants in ENPP1 that encodes ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1); and both autosomal dominant (AD) and autosomal recessive (AR) modes of inheritance have been described. 3,5,6 Hypopigmented macules start from birth to 18 months. The ultrastructural studies of hypopigmented macules have shown the presence of disproportionately large numbers of melanosomes in the cytoplasm and dendrites of melanocytes but the reduced number of melanin content in the keratinocytes suggest an impaired melanosome transfer.…”
mentioning
confidence: 99%
“…Editor, Cole disease (COLED, MIM #615522) is a rare genodermatosis characterized by dyspigmentation and punctate palmoplantar keratoderma (PPPK) of which only 13 families have been reported in the literature to date. [1][2][3][4][5][6][7][8] We report an Indian family with Cole disease with a novel pathogenic variant in ENPP1 in the somatomedin-B-like2 (SMB2) domain. A 4-year-old girl presented with slowly progressive hypopigmented lesions on upper and lower extremities (Fig.…”
mentioning
confidence: 99%
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