Results 31 to 40 of about 6,594,395 (276)
Journal of Pediatric Neurosciences, 2021 Allan Herndon Dudley syndrome (AHDS) is a rare X-linked recessive disorder due to mutation in the SLC16A2 gene, which encodes a thyroid hormone (TH) transporter that facilitates the movement of TH across the neurons. Mutation in this gene leads to a lack
Vykuntaraju Kammasandra Gowda +3 more
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Case Reports in Endocrinology, 2015 The diagnosis of central hypothyroidism is often suspected in patients with hypothalamic/pituitary pathology, in the setting of low, normal, or even slightly elevated serum TSH and low free thyroxine (FT4). We present four cases of central hypothyroidism
Kevin M. Pantalone +4 more
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Features of the nervous system lesion in primary hypothyroidism (literature review)
Mìžnarodnij Endokrinologìčnij Žurnal, 2018 The review presents the pathogenetic mechanisms of central and peripheral nervous system pathology in primary hypothyroidism. Lack of thyroid hormones leads to changes in the organization of the central nervous system, decrease in the energy supply of ...
I.I. Bilous, L.B. Pavlovych
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European Thyroid Journal, 2023 Objective: To investigate the final diagnosis and clinical outcome of pati ents referred to endocrinology in our district general hospital with biochemi cal isolated central hypothyroidism (CeH), and whether there is an association between this ...
Frederick Keen +4 more
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Hypothyroidism in children [PDF]
, 2017 Thyroid hormones are crucial for normal development of a child from early foetal life. They have an impact on the development of the central nervous system, both prenatally and up to the age of 3 years, and regulate growth and most metabolic processes.
Renata Karwowska, Karwowska, Renata
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Endocrine Connections, 2021 Hypopituitarism tends to occur in large pituitary adenomas. However, similar tumors could present with strikingly different hormonal deficiencies. In this study, we looked at MRI characteristics in non-functioning pituitary adenomas (NFPA), which could ...
Reem Al Argan +4 more
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Wolcott Rallison Syndrome: Beyond Neonatal Diabetes
Indian Pediatrics Case Reports, 2022 Background: Wolcott–Rallison Syndrome (WRS) is a rare autosomal recessive disorder characterized by permanent neonatal diabetes mellitus, skeletal dysplasia, hepatic dysfunction, and other systemic associations. Clinical Description: A 3-month-old infant
Medha Mittal +3 more
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Central Hypothyroidism in Severe Sepsis [PDF]
Acta Endocrinologica (Bucharest), 2019 A partial or complete deficiency of hormone secretion by pituitary gland (hypopituitarism) is commonly seen after a pituitary apoplexy caused by an infarction of a pituitary adenoma or pituitary hyperplasia (as in Sheehan's syndrome). Hypopituitarism may also follow surgery, when hypovolemia, anticoagulation, fat/air/bone marrow microemboli can provoke
S N, Benea +5 more
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Congenital central hypothyroidism in a neonate born to thyrotoxic mother
Journal of Integrated Health Sciences, 2016 Maternal thyrotoxicosis is associated with significant risk of low birth weight premature & small for gestational age neonates; as well as intrauterine death.
M N Rasania, P M Modi
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Acute urinary retention and hyponatremia from central hypothyroidism
, 2021 A mass arising from the pituitary gland commonly damages cells of the anterior pituitary gland and affects the secretion of gonadotropins and growth hormone.
Biniam Bearega +4 more
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