Cargando…
A case of Kallmann syndrome associated with a non-functional pituitary microadenoma
Kallmann syndrome (KS) is a form of hypogonadotropic hypogonadism in combination with a defect in sense of smell, due to abnormal migration of gonadotropin-releasing hormone-producing neurons. We report a case of a 17-year-old Tunisian male who presented with eunuchoid body proportions, absence of f...
Autores principales: | Ach, Taieb, Marmouch, Hela, Elguiche, Dorra, Achour, Asma, Marzouk, Hajer, Sayadi, Hanene, Khochtali, Ines, Golli, Mondher |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911661/ https://www.ncbi.nlm.nih.gov/pubmed/29692900 http://dx.doi.org/10.1530/EDM-18-0027 |
Ejemplares similares
-
A novel SOX10 nonsense mutation in a patient with Kallmann syndrome and Waardenburg syndrome
por: Wakabayashi, Tetsuji, et al.
Publicado: (2021) -
Multiple endocrinological failures as a clinical presentation of a metastatic lung adenocarcinoma
por: Ach, Taieb, et al.
Publicado: (2020) -
A case of pituitary apoplexy in pregnancy
por: Hayes, Aimee R, et al.
Publicado: (2014) -
Synchronous GH- and prolactin-secreting pituitary adenomas
por: Rahman, Maryam, et al.
Publicado: (2014) -
An intrasellar pituitary adenoma–gangliocytoma presenting as acromegaly
por: Lee, Melissa H, et al.
Publicado: (2017)