منابع مشابه
An Update on Subclinical Hypopituitarism
Subclinical deficiency of pituitary hormones represents an intermediate situation among normal pituitary secretion and overt hypopituitarism. Clinical hypopituitarism is associated with impaired morbidity and mortality, but there are not many studies on these topics in the subclinical setting. Moreover, clinical manifestations and diagnosis criteria are not well defined, so this entity is proba...
متن کاملHypopituitarism and Hepatitis E Genotype 3 Infection - First Case Report and Review on Immunocompetence in Hypopituitarism
Submit Manuscript | http://medcraveonline.com the tropical HEV genotypes 1 and 2 are mainly transmitted fecalorally by contaminated drinking water [1]. In the Middle East and North African regions, the seroprevalence of HEV in the general population ranged from 2.0 to 37.5% and was higher in males than in females [2]. HEV genotype 3 is also endemic in Europe and an underdiagnosed and emerging p...
متن کاملRadiation-induced hypopituitarism.
The hypothalamic-pituitary unit is a particularly radiosensitive region in the central nervous system. As a consequence, hypopituitarism commonly develops after radiation treatments for sellar and parasellar neoplasms, extrasellar brain tumours, head and neck tumours, and following whole body irradiation for systemic malignancies. Increasing tumour-related survival rates provide an expanding po...
متن کاملNeonatal Hypopituitarism: Unusual Presentation
Congenital hypopituitarism is a rare condition associated with possible serious complications and long-term neurological sequelae, if not promptly recognized and treated.1 Neonates with congenital hypopituitarism may present with or without associated developmental defects, such as ocular, midline, and genital abnormalities. They may also present with nonspecific symptoms, including hypoglycemi...
متن کامل18p- syndrome and hypopituitarism.
A patient is described with 18p- syndrome and hypopituitarism. This is the first patient with this syndrome who has been shown to benefit from growth hormone therapy. Patients with this syndrome who have growth deficiency should be considered for evaluation for hypopituitarism, if the quality of their lives would improve with an increase in stature.
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ژورنال
عنوان ژورنال: BMJ
سال: 1936
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.2.3958.984