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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

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