Empty sella, hypogonadism and hypopituitarism secondary to moyamoya disease

Tien Jen Lin; Fu Chao Hwang; Wen-Ta Chiu; Jia-Wei Lin; Shin-Han Tsai; Cheng-Kuei Chang

doi:10.1016/j.jocn.2004.05.022

Empty sella, hypogonadism and hypopituitarism secondary to moyamoya disease

Tien Jen Lin, Fu Chao Hwang, Wen-Ta Chiu, Jia-Wei Lin, Shin-Han Tsai, Cheng-Kuei Chang

研究成果: 雜誌貢獻 › 文章 › 同行評審

3 引文斯高帕斯（Scopus）

摘要

We report the case of a young male who presented at the age of 34 years with intracranial hemorrhage due to moyamoya disease. He was later diagnosed with hypogonadism and hypopituitarism. Chromosomal evaluation revealed a normal karyotype. The results of further neuroradiological studies led to the diagnosis of empty sella syndrome.

原文	英語
頁（從 - 到）	472-474
頁數	3
期刊	Journal of Clinical Neuroscience
卷	12
發行號	4
DOIs	https://doi.org/10.1016/j.jocn.2004.05.022
出版狀態	已發佈 - 5月 2005

ASJC Scopus subject areas

神經病學（臨床）
神經內科
生理學（醫學）
手術

UN SDG

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10.1016/j.jocn.2004.05.022

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title = "Empty sella, hypogonadism and hypopituitarism secondary to moyamoya disease",

abstract = "We report the case of a young male who presented at the age of 34 years with intracranial hemorrhage due to moyamoya disease. He was later diagnosed with hypogonadism and hypopituitarism. Chromosomal evaluation revealed a normal karyotype. The results of further neuroradiological studies led to the diagnosis of empty sella syndrome.",

keywords = "Empty sella syndrome, Hypogonadism, Hypopituitarism, Moyamoya disease",

author = "Lin, {Tien Jen} and Hwang, {Fu Chao} and Wen-Ta Chiu and Jia-Wei Lin and Shin-Han Tsai and Cheng-Kuei Chang",

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AU - Lin, Tien Jen

AU - Hwang, Fu Chao

AU - Chiu, Wen-Ta

AU - Lin, Jia-Wei

AU - Tsai, Shin-Han

AU - Chang, Cheng-Kuei

PY - 2005/5

Y1 - 2005/5

N2 - We report the case of a young male who presented at the age of 34 years with intracranial hemorrhage due to moyamoya disease. He was later diagnosed with hypogonadism and hypopituitarism. Chromosomal evaluation revealed a normal karyotype. The results of further neuroradiological studies led to the diagnosis of empty sella syndrome.

AB - We report the case of a young male who presented at the age of 34 years with intracranial hemorrhage due to moyamoya disease. He was later diagnosed with hypogonadism and hypopituitarism. Chromosomal evaluation revealed a normal karyotype. The results of further neuroradiological studies led to the diagnosis of empty sella syndrome.

KW - Empty sella syndrome

KW - Hypogonadism

KW - Hypopituitarism

KW - Moyamoya disease

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JO - Journal of Clinical Neuroscience

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ER -

Empty sella, hypogonadism and hypopituitarism secondary to moyamoya disease

摘要

ASJC Scopus subject areas

UN SDG

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