En sjælden form for svær overvægt hos børn og unge

Sara Østergaard Christensen; Kirsten Holm; Hanne Buciek Hove

En sjælden form for svær overvægt hos børn og unge

Sara Østergaard Christensen, Kirsten Holm, Hanne Buciek Hove

Institut for Klinisk Medicin

Abstract

A four-year-old girl was referred to a paediatric department with low height, obesity and hypothyroidism. Her paraclinical tests were characteristic with elevated P-parathyroid hormone concentration, hypothyroidism, growth hormone deficiency, abnormal phenotype with brachydactyly, tooth problems and mental retardation, which led to a suspicion of Albright's hereditary osteodystrophy (AHO). The diagnosis was verified by molecular genetic testing. Less than 1% of children with obesity have an endocrine disorder, and AHO is one of them.

Bidragets oversatte titel	A rare type of severe obesity in children and adolescents
Originalsprog	Dansk
Artikelnummer	V09160661
Tidsskrift	Ugeskrift for Laeger
Vol/bind	179
Udgave nummer	8
Antal sider	2
ISSN	0041-5782
Status	Udgivet - 1 mar. 2017

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http://ugeskriftet.dk/videnskab/en-sjaelden-form-svaer-overvaegt-hos-boern-og-unge

Citationsformater

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AU - Holm, Kirsten

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N2 - A four-year-old girl was referred to a paediatric department with low height, obesity and hypothyroidism. Her paraclinical tests were characteristic with elevated P-parathyroid hormone concentration, hypothyroidism, growth hormone deficiency, abnormal phenotype with brachydactyly, tooth problems and mental retardation, which led to a suspicion of Albright's hereditary osteodystrophy (AHO). The diagnosis was verified by molecular genetic testing. Less than 1% of children with obesity have an endocrine disorder, and AHO is one of them.

AB - A four-year-old girl was referred to a paediatric department with low height, obesity and hypothyroidism. Her paraclinical tests were characteristic with elevated P-parathyroid hormone concentration, hypothyroidism, growth hormone deficiency, abnormal phenotype with brachydactyly, tooth problems and mental retardation, which led to a suspicion of Albright's hereditary osteodystrophy (AHO). The diagnosis was verified by molecular genetic testing. Less than 1% of children with obesity have an endocrine disorder, and AHO is one of them.

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En sjælden form for svær overvægt hos børn og unge

Abstract

FN’s Verdensmål

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