Publications by authors named "Gunter Hans Neto"

Introduction: Antimicrobial resistance in leprosy is an emerging problem, and the quantitative impact of low bacilloscopic indexes (BIs) on the sensitivity of molecular tests is unknown. We aimed to evaluate the sensitivity of gene sequencing for the detection of mutations related to antimicrobial resistance in Mycobacterium leprae in patients with low BIs using an analytical model.

Methods: Patients with leprosy were included and divided into two groups depending on their BIs (≥ 2+ and < 2+).

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Introduction: Although supervised doses are essential for reducing leprosy treatment failure, the impact of specific drug interactions has rarely been assessed. This study aimed to estimate the risk of leprosy treatment suspension in patients receiving polypharmacy. METHODS We performed this case-control study in which the primary outcome was defined as the need to discontinue multibacillary leprosy treatment for at least one supervised dose, and the main risk factor was the detection of polypharmacy.

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Coatis [including Nasua nasua, the ring-tailed coati], are medium-sized mammals widely distributed in the Americas. They are social animals, whose normal diet includes insects, fruits, and small vertebrates, and rarely prey on larger sized animals. There are, to our knowledge, no reports in the medical literature of attacks on humans.

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Article Synopsis
  • Macular and lichen amyloidosis are types of primary localized cutaneous amyloidosis (PLCA), with around 10% of cases being familial, but detailed studies on these family cases are limited.* -
  • The study examined two Brazilian families, discovering that symptoms typically began in puberty with skin biopsies showing amyloid deposits; family 1 had a specific mutation in the OSMR gene, while family 2 did not.* -
  • Familial PLCA exhibits autosomal dominant inheritance with variations in clinical symptoms and mutation presence, highlighting potential insights into skin conditions related to itch and cell death.*
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Familial primary localized cutaneous amyloidosis (FPLCA) is an autosomal-dominant disorder associated with chronic skin itching and deposition of epidermal keratin filament-associated amyloid material in the dermis. FPLCA has been mapped to 5p13.1-q11.

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