| Literature DB >> 20596687 |
T Bergmann1, E G Hahn, P Lohse, I A Harsch.
Abstract
We present the case of a patient with suspected congenital hypopituitarism first diagnosed at the age of 38 years. Despite partial insufficiency of all pituitary-regulated hormonal axes, the patient never suffered from severe health problems. However, the patient was disfigured, and his intellectual and physical capacities were clearly impaired. The initiation of a hormone replacement therapy with hydrocortisone and thyroid hormones is essential in such a patient, but the substitution of sex hormones can create ethical problems.Entities:
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Year: 2010 PMID: 20596687 DOI: 10.1007/s00108-010-2615-4
Source DB: PubMed Journal: Internist (Berl) ISSN: 0020-9554 Impact factor: 0.743