Journalartikel
Autorenliste: Kamrath, Clemens
Jahr der Veröffentlichung: 2020
Seiten: C9-C12
Zeitschrift: European journal of endocrinology
Bandnummer: 182
Heftnummer: 3
ISSN: 0804-4643
eISSN: 1479-683X
Open Access Status: Bronze
DOI Link: https://doi.org/10.1530/EJE-19-0995
Verlag: Oxford University Press
Abstract:
Primary adrenal insufficiency (PAI) in children is mostly due to genetic defects. The understanding of the molecular genetics of the causes of adrenal insufficiency in the pediatric population has made significant progress during the last years. It has been shown that inherited PAI can lead to certain clinical manifestations and health problems in children beyond the adrenals. Organ dysfunctions associated with different forms of PAI in children include a wide range of organs such as gonads, brain, heart, bone, growth, bone marrow, kidney, skin, parathyroid, and thyroid. Diagnosing the correct genetic cause of PAI in children is therefore crucial to adequately control long-term treatment and follow-up in such patients.
Zitierstile
Harvard-Zitierstil: Kamrath, C. (2020) Beyond the adrenals: Organ manifestations in inherited primary adrenal insufficiency in children, European journal of endocrinology, 182(3), pp. C9-C12. https://doi.org/10.1530/EJE-19-0995
APA-Zitierstil: Kamrath, C. (2020). Beyond the adrenals: Organ manifestations in inherited primary adrenal insufficiency in children. European journal of endocrinology. 182(3), C9-C12. https://doi.org/10.1530/EJE-19-0995
Schlagwörter
ADRENOLEUKODYSTROPHY; MUTATIONS CAUSE