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The Laurence-Moon-Biedl syndrome

✍ Scribed by Ross, C. F. ;Crome, L. ;Mackenzie, D. Y.

Publisher: Wiley (John Wiley & Sons)
Year: 1956
Tongue: English
Weight: 861 KB
Volume: 72
Category: Article
ISSN: 0368-3494
DOI: 10.1002/path.1700720122

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## 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

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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 importan

Laurence-Moon-Biedl syndrome (?) and Pra

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Mental retardation, hypogonadism, obesity, and abnormal blood sugar regulation were common findings in two siblings. In addition, the 17-year-old female patient showed short stature, muscular hypotonia in infancy, and small hands with tapering fingers suggesting Prader-Willi syndrome, and the 12-yea