Literature DB >> 20596687

[38 year-old patient with suspected congenital hormonal dysfunction].

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.

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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


  5 in total

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Review 2.  Testosterone deficiency and replacement.

Authors:  S Howell; S Shalet
Journal:  Horm Res       Date:  2001

3.  Influence of timing and dose of thyroid hormone replacement on mental, psychomotor, and behavioral development in children with congenital hypothyroidism.

Authors:  Jacoba J Bongers-Schokking; Sabine M P F de Muinck Keizer-Schrama
Journal:  J Pediatr       Date:  2005-12       Impact factor: 4.406

4.  Long-term follow-up of childhood-onset hypopituitarism in patients with the PROP-1 gene mutation.

Authors:  Marianne E Pavel; Johannes Hensen; Roland Pfäffle; Eckhart G Hahn; Helmuth G Dörr
Journal:  Horm Res       Date:  2003

Review 5.  Evolving issues in male hypogonadism: evaluation, management, and related comorbidities.

Authors:  Martin M Miner; Richard Sadovsky
Journal:  Cleve Clin J Med       Date:  2007-05       Impact factor: 2.321

  5 in total

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