Results 91 to 100 of about 22,586 (217)
ABSTRACT Non‐syndromic paucity of interlobular bile ducts (NSPIBD) is a rare cause of neonatal cholestasis, often presenting with clinical features similar to extrahepatic biliary atresia. This report presents a case of NSPIBD in an infant with Down syndrome who exhibited jaundice and pale stools.
Pui Ling Thong +3 more
wiley +1 more source
Clinical Profile of Patients with Hypopituitarism in a Tertiary Care Centre in Central India
Introduction: Hypopituitarism is a serious endocrine illness with life-threatening implications. There is a lack of reliable Indian epidemiological data, with very few studies on hypopituitarism across the country.
Vinay R. Pandit +4 more
doaj +1 more source
The monosomy 18p-syndrome refers to an extremely rare disorder (1:50,000 live-born infants). Congenital hypopituitarism is one of the manifestations of this syndrome in 13% of cases. The rarity of this pathology causes difficulties in the early detection
A. V. Degtyareva +3 more
doaj +1 more source
Penile length and anogenital distance in male newborns from different Iranian ethnicities in Golestan Province [PDF]
Background: Anogenital distance (AGD) is a feasible and accepted parameter of exogenous or endogenous androgens effects on development of reproductive ...
Alaee, E. +2 more
core +1 more source
Severe Headache and Acute Blindness: A Case of Pituitary Apoplexy
ABSTRACT Pituitary apoplexy is a rare, life‐threatening syndrome that commonly occurs in the adenomatous pituitary gland. It presents with a myriad of severe neuroendocrine and ophthalmological signs and symptoms. Early diagnosis and prompt treatment are vital in the management of pituitary apoplexy.
Abdul‐Rahman Faiza +4 more
wiley +1 more source
Characteristics of NAFLD Based on Hypopituitarism
Background. Hypopituitarism and hypothalamic disorders, which induce central obesity and appetite disorder, are associated with nonalcoholic fatty liver disease (NAFLD).
Kazuhisa Kodama +7 more
doaj +1 more source
ABSTRACT Introduction Pituitary apoplexy represents an uncommon endocrine emergency with potentially life‐threatening consequences. Gonadotropin‐releasing hormone agonist used for prostate cancer has the potential to induce pituitary apoplexy, particularly in the setting of a preexisting pituitary adenoma.
Masaaki Fujimura +5 more
wiley +1 more source
Introdução: O hipopituitarismo é caracterizado por insuficiência da secreção hormonal hipófisária. A clínica é variável e depende da etiologia, evolução temporal e hormonas envolvi- das.
Afonso, Ariana +6 more
core
Lymphocytic Hypophysitis [PDF]
A 59 year-old female presented with visual problems in 2006, and was initially diagnosed with a pituitary macroadenoma on MRI (Figure 1). Preoperatively, the pituitary lesion decreased in size after the patient was started on steroids, raising the ...
Evans, James J. +4 more
core +2 more sources
Pituitary dysfunction following traumatic brain injury: clinical perspectives
Fatih Tanriverdi, Fahrettin Kelestimur Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey Abstract: Traumatic brain injury (TBI) is a well recognized public health problem worldwide.
Tanriverdi F, Kelestimur F
doaj

