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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004922naa a2200829 4500
001oai:gup.ub.gu.se/325045
003SwePub
008240528s2023 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:152126553
0247 a https://gup.ub.gu.se/publication/3250452 URI
0247 a https://doi.org/10.1210/endrev/bnad0022 DOI
0247 a http://kipublications.ki.se/Default.aspx?queryparsed=id:1521265532 URI
040 a (SwePub)gud (SwePub)ki
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
1001 a Hokken-Koelega, A. C. S.u Karolinska Institutet4 aut
2451 0a International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early Adulthood
264 c 2023-01-13
264 1b The Endocrine Society,c 2023
520 a This International Consensus Guideline was developed by experts in the field of small for gestational age (SGA) of 10 pediatric endocrine societies worldwide. A consensus meeting was held and 1300 articles formed the basis for discussions. All experts voted about the strengths of the recommendations. The guideline gives new and clinically relevant insights into the etiology of short stature after SGA birth, including novel knowledge about (epi)genetic causes. Further, it presents long-term consequences of SGA birth and also reviews new treatment options, including treatment with gonadotropin-releasing hormone agonist (GnRHa) in addition to growth hormone (GH) treatment, as well as the metabolic and cardiovascular health of young adults born SGA after cessation of childhood GH treatment in comparison with appropriate control groups. To diagnose SGA, accurate anthropometry and use of national growth charts are recommended. Follow-up in early life is warranted and neurodevelopment evaluation in those at risk. Excessive postnatal weight gain should be avoided, as this is associated with an unfavorable cardiometabolic health profile in adulthood. Children born SGA with persistent short stature < -2.5 SDS at age 2 years or < -2 SDS at 3 to 4 years of age, should be referred for diagnostic workup. In case of dysmorphic features, major malformations, microcephaly, developmental delay, intellectual disability, and/or signs of skeletal dysplasia, genetic testing should be considered. Treatment with 0.033 to 0.067 mg GH/kg/day is recommended in case of persistent short stature at age of 3 to 4 years. Adding GnRHa treatment could be considered when short adult height is expected at pubertal onset. All young adults born SGA require counseling to adopt a healthy lifestyle.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Pediatrik0 (SwePub)302212 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Pediatrics0 (SwePub)302212 hsv//eng
653 a SGA
653 a etiology
653 a consequences
653 a management
653 a genetics
653 a GH
653 a growth-hormone treatment
653 a bone-mineral density
653 a catch-up growth
653 a cardiovascular risk-factors
653 a copy number variants
653 a long-term mortality
653 a children born sga
653 a quality-of-life
653 a reduced insulin sensitivity
653 a central
653 a precocious puberty
653 a Endocrinology & Metabolism
7001 a van der Steen, M.4 aut
7001 a Boguszewski, M. C. S.4 aut
7001 a Cianfarani, S.4 aut
7001 a Dahlgren, Jovanna,d 1964u Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics4 aut0 (Swepub:gu)xdajov
7001 a Horikawa, R.4 aut
7001 a Mericq, V.4 aut
7001 a Rapaport, R.4 aut
7001 a Alherbish, A.4 aut
7001 a Braslavsky, D.4 aut
7001 a Charmandari, E.4 aut
7001 a Chernausek, S. D.4 aut
7001 a Cutfield, W. S.4 aut
7001 a Dauber, A.4 aut
7001 a Deeb, A.4 aut
7001 a Goedegebuure, W. J.4 aut
7001 a Hofman, P. L.4 aut
7001 a Isganatis, E.4 aut
7001 a Jorge, A. A.4 aut
7001 a Kanaka-Gantenbein, C.4 aut
7001 a Kashimada, K.4 aut
7001 a Khadilkar, V.4 aut
7001 a Luo, X. P.4 aut
7001 a Mathai, S.4 aut
7001 a Nakano, Y.4 aut
7001 a Yau, M.4 aut
7102 a Karolinska Institutetb Institutionen för kliniska vetenskaper, Avdelningen för pediatrik4 org
7730 t Endocrine Reviewsd : The Endocrine Societyg 44:3, s. 539-565q 44:3<539-565x 0163-769Xx 1945-7189
8564 8u https://gup.ub.gu.se/publication/325045
8564 8u https://doi.org/10.1210/endrev/bnad002
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:152126553

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