نتایج جستجو برای: congenital hypopituitarism

تعداد نتایج: 121663  

Journal: :Hormone research 2007
Mark E Molitch Mary P Gillam

BACKGROUND Lymphocytic hypophysitis is a disorder of the pituitary gland that presents as a sellar mass lesion and/or hypopituitarism. It causes pituicyte destruction and hypopituitarism and is speculated to have an autoimmune basis. DIAGNOSIS Lymphocytic hypophysitis should be considered in the differential diagnosis of pituitary masses and/or hypopituitarism in females who are pregnant or i...

Journal: :QJM : monthly journal of the Association of Physicians 2014
V Wilson A Mallipedhi J W Stephens R M Redfern D E Price

BACKGROUND Hypopituitarism in the absence of a history of pituitary pathology or abnormal pituitary imaging is rare. AIM To identify the cause of hypopituitarism in individuals in whom pituitary imaging was normal. DESIGN Retrospective analysis of electronic patient record. METHOD A review of the pituitary function in the 506 patients on the Morriston Hospital pituitary database revealed ...

Journal: :The Journal of clinical endocrinology and metabolism 2002
Ravinder Goswami Narayana Kochupillai Patricia A Crock Abdul Jaleel Nandita Gupta

Postpartum hemorrhage (PPH) is a frequent complication of pregnancy in India. Sheehan's description of postpartum hypopituitarism promoted the belief that PPH leads to necrosis of the enlarged pituitary gland of pregnancy and hypopituitarism. However, slow clinical progression suggests factors other than ischemia in its pathogenesis. Tissue necrosis could release sequestered antigens, triggerin...

Journal: :Journal of diabetes and endocrine practice 2023

Abstract Pituitary hormones are responsible for the regulation of growth, development, metabolism, reproduction, and homeostasis. Hypopituitarism is a condition that defined as partial or complete insufficiency anterior pituitary hormone secretion, rarely, posterior secretion. This can result from diseases gland hypothalamus. The annual incidence hypopituitarism has been estimated to be 4.2 per...

Journal: :Journal of medical genetics 1992
H G Artman C A Morris A D Stock

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.

2006
H B NEUSTEIN

Optic nerve hypoplasia with hypopituitarism and intact septum pellucidum is a variant of septo-optic dysplasia or deMorsier's syndrome.' Although neonatal jaundice has been seen with this syndrome, the association with severe prolonged cholestatic jaundice has not been emphasised. We describe three patients who presented with cholestatic jaundice and were found to have optic nerve hypoplasia an...

2017
Agnethe Berglund Morten Olsen Marianne Andersen Eigil Husted Nielsen Ulla Feldt-Rasmussen Caroline Kistorp Claus Højbjerg Gravholt Kirstine Stochhholm

OBJECTIVE Routinely collected health data may be valuable sources for conducting research. This study aimed to evaluate the validity of algorithms detecting hypopituitary patients in the Danish National Patient Registry (DNPR) using medical records as reference standard. STUDY DESIGN AND SETTING Patients with International Classification of Diseases (10th edition [ICD-10]) diagnoses of hypopi...

Journal: :European journal of endocrinology 2011
N E Kokshoorn J W A Smit W A Nieuwlaat J Tiemensma P H Bisschop R Groote Veldman F Roelfsema A A M Franken M J E Wassenaar N R Biermasz J A Romijn A M Pereira

OBJECTIVE Hypopituitarism after traumatic brain injury (TBI) is considered to be a prevalent condition. However, prevalence rates differ considerably among reported studies, due to differences in definitions, endocrine assessments of hypopituitarism, and confounding factors, such as timing of evaluation and the severity of the trauma. Aim To evaluate the prevalence of hypopituitarism in a large...

Journal: :The Journal of clinical endocrinology and metabolism 2010
Giuseppe Bellastella Mario Rotondi Elena Pane Assunta Dello Iacovo Barbara Pirali Liliana Dalla Mora Alberto Falorni Antonio Agostino Sinisi Antonio Bizzarro Annamaria Colao Luca Chiovato Annamaria De Bellis

CONTEXT Antipituitary antibodies (APA) are frequently present in patients with autoimmune polyendocrine syndrome (APS). DESIGN The aim was to evaluate the predictive value of APA for the occurrence of hypopituitarism. A total of 149 APA-positive and 50 APA-negative patients with APS and normal pituitary function were longitudinally studied for 5 yr. METHODS APA, by indirect immunofluorescen...

Journal: :Postgraduate medical journal 1988
T Beringer B McClements I Weir D Gilmore L Kennedy

Two cases of primary hypothyroidism with hypopituitarism in elderly patients are reported. The elevated levels of thyroid stimulating hormone led to delay in the recognition of accompanying pituitary failure. Elderly patients should not be commenced on thyroxine replacement therapy until the possibility of hypopituitarism and cortisol deficiency has been excluded.

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