Anosmia
Mostrando 1-12 de 51 artigos, teses e dissertações.
-
1. Anosmia in COVID-19 Patients: Can We Predict the Severity of Chest Manifestations?
Abstract Introduction Anosmia is one of the common symptoms of COVID-19, the link between severity of chest infection and anosmia was investigated by few studies. Objectives To find an association between anosmia and severity of chest infection. Methods An analysis of patients admitted to isolation hospital of our university with confirmed polymerase chai
International Archives of Otorhinolaryngology. Publicado em: 2023
-
2. Anosmia in Alkaline Battery Workers
The sense of smell of 106 alkaline battery workmen exposed at their work to cadmium and nickel dust has been compared with a control group of 84 men matched for age. The battery workers reported significantly more anosmia than the controls (15% to zero) and did less well in the phenol smelling test (27·3% to 4·8%). Cadmium proteinuria was found in 17 of th
-
3. Anosmia/Hyposmia is a Good Predictor of Coronavirus Disease 2019 (COVID-19) Infection: A Meta-Analysis
Abstract Introduction The number of positive cases and deaths from the coronavirus disease 2019 (COVID-19) is still increasing. The early detection of the disease is very important. Olfactory dysfunction has been reported as the main symptom in part of the patients. Objective To analyze the potential usefulness of anosmia or hyposmia in the detection of th
Int. Arch. Otorhinolaryngol.. Publicado em: 2021-01
-
4. The Basal Cell Naevus Syndrome: Report of a Family with Anosmia and a Case of Hypogonadotrophic Hypopituitarism
A family with the naevoid basal cell carcinoma syndrome is described. Three affected members in one sibship suffered from anosmia. One member has shown a most severe constellation of defects including cataracts, hypertelorism, and anosmia, together with hypogonadism secondary to partial pituitary dysfunction. It is suggested that this latter also represents
-
5. Hipogonadismo hipogonadotrófico e anosmia: síndrome de Kallmann
A síndrome de Kallmann caracteriza-se pela associação de hipogonadismo hipogonadotrófico à anosmia ou hiposmia. É causada por um defeito na migração dos neurônios que produzem o GnRH e dos neurônios que formam os nervos olfatórios. A doença afeta somente a secreção de gonadotrofina, sendo que todos os outros hormônios hipofisários são secret
Revista Brasileira de Otorrinolaringologia. Publicado em: 01/11/2001
-
6. Pathophysiological relationship between COVID-19 and olfactory dysfunction: A systematic review
Resumo Introdução SARS‐CoV‐2 é o patógeno da Covid‐19. O vírus é composto pela proteína spike (espigão), a membrana e o envelope. No olfato fisiológico, as substâncias odoríferas se ligam a proteínas secretadas pelas células sustentaculares para serem processadas pelos neurônios receptores olfativos. O distúrbio olfativo é uma das prin
Brazilian Journal of Otorhinolaryngology. Publicado em: 2022
-
7. Causes of anosmia.
-
8. Causes of Anosmia
-
9. A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).
A case of Kallmann's syndrome in a male is reported. Besides the classical picture of hypogonadotrophic hypogonadism (demonstrated both by endocrine investigation and a testicular biopsy) with anosmia, a number of other unusual features are present including gynaecomastia, agencies of the anterior brachial muscles, some dental abnormalities, and dyschromatop
-
10. Ageusia e anosmia na vigência de tratamento com leflunomida para artrite reumatóide (AR)
Revista Brasileira de Reumatologia. Publicado em: 2005-12
-
11. Cytogenetic analysis and detection of KAL-1 gene deletion with fluorescence in situ hybridization (FISH) in patients with Kallmann syndrome
A síndrome de Kallmann (SK) é caracterizada clinicamente pela associação de hipogonadismo hipogonadotrófico e anosmia ou hiposmia, para a qual três modos de herança foram descritos: ligada ao X, autossômica dominante e recessiva. O gene KAL-1, responsável pela forma da síndrome ligada ao X, foi isolado e sua organização éxon-íntron determinada.
Arquivos Brasileiros de Endocrinologia & Metabologia. Publicado em: 2001-12
-
12. Familial spastic paraplegia with Kallmann's syndrome.
A sibship is reported in which two males have spastic paraparesis and Kallmann's syndrome (hypogonadotrophic hypogonadism and anosmia). One of the brothers also is color blind. The association of familial spastic paraplegia and Kallmann's syndrome has not been described previously.