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Review
. 2018;22(3):280-283.
doi: 10.34763/devperiodmed.20182203.280283.

Cortisol deficiency as a rare cause of neonatal cholestasis

Affiliations
Review

Cortisol deficiency as a rare cause of neonatal cholestasis

Patryk Lipiński et al. Dev Period Med. 2018.

Abstract

Cortisol deficiency constitutes a rare cause of neonatal cholestasis. The aim of this manuscript was to present the pathogenesis of cortisol deficiency in neonatal cholestasis. The authors also present the characteristics of selected disorders resulting in cortisol deficiency.

Keywords: cholestasis; cortisol; familial glucocorticoid deficiency; multiple pituitary hormone deficiency; pituitary stalk interruption syndrome.

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Conflict of interest statement

Conflicts of interest

Konflikt interesu/Conflicts of interest

Autorzy pracy nie zgłaszają konfliktu interesów.

The Authors declare no conflict of interest.

Figures

Ryc. 1
Ryc. 1
Schemat transportu kwasów żółciowych [25, opublikowano za zgodą autora]. Objaśnienia: AL – aminofosfolipidy, PC – fosfatydylocholina, BA – kwasy żółciowe, OA – aniony organiczne, FIC1 – pompa odpowiadająca za przezbłonowy transport amino-fosfolipidów, BSEP – pompa eksportująca sole kwasów żółciowych, MDR3 – przenośnik fosfatydylocholiny, MRP2 – pompa transportująca kwasy żółciowe do krążenia ogólnego. Fig. 1. Schematic presentation of bile acid transport [25]. AL – aminophospholipids, PC – phosphatidylocholine, BA – bile acids, OA – organic anions, FIC1 – aminophospholipid transporter, BSEP – bile salt export pump, MDR3 – multidrug resistance protein 3, MRP2 – multidrug resistance associated protein.

References

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