Delayed diagnosis of congenital hypopituitarism associated with low socio-economic status and/or migration
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-019-03489-3.pdf
Reference12 articles.
1. Arrigo T, Crisafulli G, Salamone A, Cucinotta D, de Luca F (1994) Adult height exceeding target height in a patient with congenital panhypopituitarism diagnosed after the age of 25 years. J Pediatr Endocrinol 7:269–272
2. Badawy SZ, Pisarska MD, Wasenko JJ, Buran JJ (1994) Congenital hypopituitarism as part of suprasellar dysplasia. A case report. J Reprod Med 39:643–648
3. Castinetti F, Reynaud R, Saveanu A, Jullien N, Quentien MH, Rochette C, Barlier A, Enjalbert A, Brue T (2016) Mechanisms in endocrinology: an update in the genetic aetiologies of combined pituitary hormone deficiency. Eur J Endocrinol 174:R239–R247. https://doi.org/10.1530/EJE-15-1095
4. Den Ouden DT, Kroon M, Hoogland PH et al (2002) A 43-year-old male with untreated panhypopituitarism due to absence of the pituitary stalk: from dwarf to giant. J Clin Endocrinol Metab 87:5430–5434. https://doi.org/10.1210/jc.2002-020672
5. Grumbach MM (2005) A window of opportunity: the diagnosis of gonadotropin deficiency in the male infant. J Clin Endocrinol Metab. 90(5):3122–3127
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young Adults;The Journal of Clinical Endocrinology & Metabolism;2022-10-06
2. Delayed Diagnosis of Congenital Combined Pituitary Hormone Deficiency including Severe Growth Hormone Deficiency in Children with Persistent Neonatal Hypoglycemia—Case Reports and Review;International Journal of Molecular Sciences;2022-09-21
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