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Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment

Hypopituitarism is defined as a decreased release of hypophyseal hormones, which may be caused by disease of the pituitary gland disease or hypothalamus. The clinical findings of neonatal hypopituitarism depend on the causes and on presence and extent of hormonal deficiency. Patients may be asymptom...

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Detalles Bibliográficos
Autores principales: Kurtoğlu, Selim, Özdemir, Ahmet, Hatipoğlu, Nihal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398195/
https://www.ncbi.nlm.nih.gov/pubmed/29739730
http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0036
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author Kurtoğlu, Selim
Özdemir, Ahmet
Hatipoğlu, Nihal
author_facet Kurtoğlu, Selim
Özdemir, Ahmet
Hatipoğlu, Nihal
author_sort Kurtoğlu, Selim
collection PubMed
description Hypopituitarism is defined as a decreased release of hypophyseal hormones, which may be caused by disease of the pituitary gland disease or hypothalamus. The clinical findings of neonatal hypopituitarism depend on the causes and on presence and extent of hormonal deficiency. Patients may be asymptomatic or may demonstrate non-specific symptoms, but may still be at risk for development of pituitary hormone deficiency over time. Patient history, physical examination, endocrinological, radiological and genetic evaluations are all important for early diagnosis and treatment. The aim of this paper was to present a review of etiological factors, clinical findings, diagnosis and treatment approaches in neonatal hypopituitarism.
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spelling pubmed-63981952019-03-22 Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment Kurtoğlu, Selim Özdemir, Ahmet Hatipoğlu, Nihal J Clin Res Pediatr Endocrinol Review Hypopituitarism is defined as a decreased release of hypophyseal hormones, which may be caused by disease of the pituitary gland disease or hypothalamus. The clinical findings of neonatal hypopituitarism depend on the causes and on presence and extent of hormonal deficiency. Patients may be asymptomatic or may demonstrate non-specific symptoms, but may still be at risk for development of pituitary hormone deficiency over time. Patient history, physical examination, endocrinological, radiological and genetic evaluations are all important for early diagnosis and treatment. The aim of this paper was to present a review of etiological factors, clinical findings, diagnosis and treatment approaches in neonatal hypopituitarism. Galenos Publishing 2019-03 2019-02-20 /pmc/articles/PMC6398195/ /pubmed/29739730 http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0036 Text en ©Copyright 2019 by Turkish Pediatric Endocrinology and Diabetes Society | The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Kurtoğlu, Selim
Özdemir, Ahmet
Hatipoğlu, Nihal
Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title_full Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title_fullStr Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title_full_unstemmed Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title_short Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
title_sort neonatal hypopituitarism: approaches to diagnosis and treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398195/
https://www.ncbi.nlm.nih.gov/pubmed/29739730
http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0036
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