## ABSTRACT We report a 30‐year‐old European (Ashkenazi Jewish) male with Laurence–Moon–Biedl syndrome (Bardet–Biedl type) who was hospitalized because of severe recalcitrant plaque‐type psoriasis. Laurence–Moon–Biedl syndrome has been shown to be linked to the chromosome 11q region in the majority
✦ LIBER ✦
Laurence-Moon-Biedl syndrome associated with diabetes insipidus neurohormonalis
✍ Scribed by Peter Koepp
- Publisher
- Springer
- Year
- 1975
- Tongue
- English
- Weight
- 181 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0340-6997
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✦ Synopsis
The case of a girl with Laurence-Moon-Biedl syndrome without polydactyly is described. Additional features were small stature, diabetes insipidus neurohormonalis and a renal disorder. The diabetes insipidus neurohormonalis was successfully treated with a new vasopressin analogue, DDAVP. The importance of renal studies in patients with Laurence-Moon-Biedl syndrome is emphasized.
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