Eight rare urinary disorders in a patient with Kallmann syndrome: A case report

RATIONALE: Kallmann syndrome (KS) is a rare inherited genetic disorder characterized by hypogonadotropic hypogonadism and hyposmia/anosmia. Early diagnosis is the key to timely treatment and improvement of prognosis in patients with KS. As the most common complication of KS, renal agenesis can provi...

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Detalles Bibliográficos
Autores principales: Tian, Huining, Yan, Zi, Lv, You, Sun, Lin, Gang, Xiaokun, Wang, Guixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581024/
https://www.ncbi.nlm.nih.gov/pubmed/33120852
http://dx.doi.org/10.1097/MD.0000000000022936

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581024/
https://www.ncbi.nlm.nih.gov/pubmed/33120852
http://dx.doi.org/10.1097/MD.0000000000022936

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