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1.
Nurs Clin North Am ; 53(3): 395-405, 2018 09.
Article in English | MEDLINE | ID: mdl-30100005

ABSTRACT

Hypogonadism is a clinical syndrome that results in hormone deficiency in men and women. Primary hypogonadism is caused by gonadal (testicular or ovarian) failure. Secondary hypogonadism is the result of a dysfunction within the hypothalamus and/or pituitary. Diagnosis of hypogonadism requires a comprehensive health history, evaluation of the signs and symptoms, complete physical examination, as well as laboratory and diagnostic testing for both sexes. Hormone replacement is the hallmark of hypogonadism treatment. Restoring and/or maintaining quality of life is a major consideration in the management of patients with hypogonadism.


Subject(s)
Hypogonadism/diagnosis , Female , Hormone Replacement Therapy , Humans , Hypogonadism/nursing , Hypogonadism/psychology , Hypogonadism/therapy , Kallmann Syndrome/diagnosis , Kallmann Syndrome/nursing , Kallmann Syndrome/psychology , Kallmann Syndrome/therapy , Klinefelter Syndrome/diagnosis , Klinefelter Syndrome/nursing , Klinefelter Syndrome/psychology , Klinefelter Syndrome/therapy , Male , Quality of Life , Turner Syndrome/diagnosis , Turner Syndrome/nursing , Turner Syndrome/psychology , Turner Syndrome/therapy
2.
Pediatr Endocrinol Rev ; 14(Suppl 2): 462-471, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28647951

ABSTRACT

47,XXY (Klinefelter Syndrome) is associated with a spectrum of complex clinical needs that are associated with variable physical, neurocognitive and psychosocial aspects. For patients and families affected by this sex chromosome trisomy, navigation of health care services is difficult due to lack of 47,XXY awareness among many health care providers and little evidence to support endocrine and additional treatment plans. While endocrine management of androgen deficiency has been the mainstay of treatment for patients from puberty through adulthood, testosterone replacement, alone, fails to mitigate many symptoms and issues. Prior to the onset of puberty, boys with 47,XXY often do not receive interdisciplinary evaluations and treatment. Since multiple health and ancillary therapeutic services are required for the management of 47,XXY, patients and families often experience disjointed and uncoordinated care. We discuss complexities of caring for patients with 47,XXY and the benefit of integrating advanced practice nursing and medical perspectives to improve care delivery.


Subject(s)
Advanced Practice Nursing , Klinefelter Syndrome/nursing , Klinefelter Syndrome/therapy , Quality of Health Care , Advanced Practice Nursing/methods , Advanced Practice Nursing/standards , Cognition/physiology , Genetic Heterogeneity , Humans , Klinefelter Syndrome/diagnosis , Klinefelter Syndrome/psychology , Mental Disorders/complications , Mental Disorders/epidemiology , Mental Disorders/therapy , Phenotype , Quality of Health Care/standards , Social Behavior Disorders/complications , Social Behavior Disorders/epidemiology , Social Behavior Disorders/therapy
3.
Nurse Pract ; 25(5): 116, 2000 May.
Article in English | MEDLINE | ID: mdl-10826139
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