Væksthormonmangel hos børn

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Standard

Væksthormonmangel hos børn. / Nielsen, Jon; Jensen, Rikke Beck; Juul, Anders.

I: Ugeskrift for Laeger, Bind 176, Nr. 25, V12130706, 2014, s. 2-6.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Nielsen, J, Jensen, RB & Juul, A 2014, 'Væksthormonmangel hos børn', Ugeskrift for Laeger, bind 176, nr. 25, V12130706, s. 2-6.

APA

Nielsen, J., Jensen, R. B., & Juul, A. (2014). Væksthormonmangel hos børn. Ugeskrift for Laeger, 176(25), 2-6. [V12130706].

Vancouver

Nielsen J, Jensen RB, Juul A. Væksthormonmangel hos børn. Ugeskrift for Laeger. 2014;176(25):2-6. V12130706.

Author

Nielsen, Jon ; Jensen, Rikke Beck ; Juul, Anders. / Væksthormonmangel hos børn. I: Ugeskrift for Laeger. 2014 ; Bind 176, Nr. 25. s. 2-6.

Bibtex

@article{b9852840d81949d9ae8cd3d6ecd6ad14,
title = "V{\ae}ksthormonmangel hos b{\o}rn",
abstract = "Growth hormone (GH) deficiency may be of congenital origin and may present with typical clinical signs and symptoms very early in postnatal life, but may also present later during childhood with growth deceleration. In a short-statured child suspected of GH deficiency, diagnostic procedures include appropriate auxological measurements using updated national growth references, bone age determination, and biochemical evaluation. GH dose is adjusted every three months based on height changes and serum insulin-like growth factor-I concentration. After cessation of linear growth, GH secretion should be re-evaluated during transitional care from a paediatric to an adult endocrinological setting.",
author = "Jon Nielsen and Jensen, {Rikke Beck} and Anders Juul",
year = "2014",
language = "Dansk",
volume = "176",
pages = "2--6",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "25",

}

RIS

TY - JOUR

T1 - Væksthormonmangel hos børn

AU - Nielsen, Jon

AU - Jensen, Rikke Beck

AU - Juul, Anders

PY - 2014

Y1 - 2014

N2 - Growth hormone (GH) deficiency may be of congenital origin and may present with typical clinical signs and symptoms very early in postnatal life, but may also present later during childhood with growth deceleration. In a short-statured child suspected of GH deficiency, diagnostic procedures include appropriate auxological measurements using updated national growth references, bone age determination, and biochemical evaluation. GH dose is adjusted every three months based on height changes and serum insulin-like growth factor-I concentration. After cessation of linear growth, GH secretion should be re-evaluated during transitional care from a paediatric to an adult endocrinological setting.

AB - Growth hormone (GH) deficiency may be of congenital origin and may present with typical clinical signs and symptoms very early in postnatal life, but may also present later during childhood with growth deceleration. In a short-statured child suspected of GH deficiency, diagnostic procedures include appropriate auxological measurements using updated national growth references, bone age determination, and biochemical evaluation. GH dose is adjusted every three months based on height changes and serum insulin-like growth factor-I concentration. After cessation of linear growth, GH secretion should be re-evaluated during transitional care from a paediatric to an adult endocrinological setting.

M3 - Tidsskriftartikel

C2 - 25352279

VL - 176

SP - 2

EP - 6

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 25

M1 - V12130706

ER -

ID: 137502582