Results 11 to 20 of about 1,442,730 (143)

Neonatal Cholestasis: A Rare and Unusual Presentation of Pituitary Stalk Interruption Syndrome [PDF]

open access: yesCase Reports in Endocrinology, 2021
Pituitary stalk interruption syndrome (PSIS) is a very rare entity, and the clinical manifestations are nonspecific. Neonatal cholestasis due to endocrine disorders is rare and poorly recognized.
R. El Qadiry   +4 more
doaj   +3 more sources

Pituitary Stalk Interruption Syndrome with Excessive Height Growth Combined with Congenital Absence of the Uterus and Ovaries: A Rare Case Report and Review of the Literature [PDF]

open access: yesDiabetes, Metabolic Syndrome and Obesity
Rongqian Wu,1– 3 Jixiong Xu1– 3 1Department of Endocrinology and Metabolism, The 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, People’s Republic of China; 2Jiangxi Clinical Research Center for Endocrine and Metabolic ...
Wu R, Xu J
doaj   +4 more sources

Clinical Features and Analysis in Pituitary Stalk Interruption Syndrome [PDF]

open access: yesInternational Journal of Endocrinology
Objective. Pituitary stalk interruption syndrome (PSIS) is characterized by the absence of pituitary stalk, pituitary hypoplasia, and ectopic posterior pituitary.
Qiuxuan Guo, Jing Zhao, Shuang Yu
doaj   +3 more sources

Pituitary stalk interruption syndrome is characterized by genetic heterogeneity. [PDF]

open access: yesPLoS ONE, 2020
Pituitary stalk interruption syndrome is a rare disorder characterized by an absent or ectopic posterior pituitary, interrupted pituitary stalk and anterior pituitary hypoplasia, as well as in some cases, a range of heterogeneous somatic anomalies.
Raja Brauner   +3 more
doaj   +3 more sources

Importance of Magnetic Resonance Imaging in Pituitary Stalk Interruption Syndrome

open access: yesEndocrinology Research and Practice, 2019
Objective: To evaluate the importance of magnetic resonance imaging in the treatment and follow-up of patients with pituitary stalk interruption syndrome.
Eren GÜRKAN   +4 more
doaj   +3 more sources

A Rare Cause of Pituitary Deficiency: Pituitary Stalk Interruption Syndrome and Magnetic Resonance Imaging Findings [PDF]

open access: yesForbes Tıp Dergisi, 2020
Pituitary stalk interruption syndrome is a rare disease characterized by a deficiency of adenohypophyseal hormones. Clinical presentation usually occurs in childhood or in the second decade of life. The severity of hormonal deficiency is variable. It may
Atilla Hikmet Çilengir   +3 more
doaj   +2 more sources

Two Cases of Pituitary Stalk Interruption Syndrome in Syrian Children

open access: yesCase Reports in Endocrinology, 2020
Pituitary stalk interruption syndrome (PSIS) is an extremely rare cause of growth failure and delayed puberty. It can be diagnosed by magnetic resonance imaging (MRI) of the hypothalamus and pituitary gland, showing an ectopic or absent posterior ...
Ibrahim Alali, Reem Saad, Younes Kabalan
doaj   +2 more sources

Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2017
Pituitary stalk interruption syndrome (PSIS) involves the occurrence of a thin or absent pituitary stalk, hypoplasia of the adenohypophysis, and ectopic neurohypophysis. Diagnosis is confirmed using magnetic resonance imaging.
Kyung Mi Jang, Cheol Woo Ko
doaj   +2 more sources

A Novel Missense Mutation in Human Receptor Roundabout-1 (ROBO1) Gene Associated with Pituitary Stalk Interruption Syndrome

open access: yesJCRPE, 2020
Pituitary stalk interruption syndrome (PSIS) is characterized by the association of an absent or thin pituitary stalk, an absent or hypoplastic anterior pituitary lobe and an ectopic posterior pituitary (EPP) lobe.
Ziqin Liu, Xiaobo Chen
doaj   +2 more sources

Pituitary stalk interruption syndrome presenting in a euthyroid adult with short stature [PDF]

open access: yesRadiology Case Reports, 2018
Pituitary stalk interruption syndrome (PSIS) is a distinct and rare clinical entity responsible for congenital hypopituitarism resulting in deficiency of pituitary hormones with deficiency of the growth hormone (100%) and gonadotropins (97.2%) being its ...
Atif Nawaz, MBBS, FCPS-I, FRCR-I   +2 more
doaj   +3 more sources

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