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 |
| Tidsskrift | Ugeskrift for Laeger |
| Vol/bind | 179 |
| Udgave nummer | 11 |
| Sider (fra-til) | 985 |
| ISSN | 0041-5782 |
| Status | Udgivet - 20 feb. 2017 |