期刊
CLINICS IN PERINATOLOGY
卷 45, 期 1, 页码 75-+出版社
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.clp.2017.11.001
关键词
Hypopituitarism; Hypoglycemia; Cholestasis; Growth hormone; MRI; Pituitary stalk; Guidelines
Mutations of growth hormone genes and pituitary transcription factors account for a small proportion of cases of severe congenital hypopituitarism. Most cases show characteristic MRI findings of pituitary stalk interruption syndrome. Clinical suspicion should prompt assessment of cortisol, free T4, thyroid-stimulating hormone, and growth hormone levels together with MRI of the hypothalamic and pituitary regions.
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