How to Cite this Article: Posmyk R, Leśniewicz R, Chorąży M, Wołczyński S. 2011. New case of Primrose syndrome with mild intellectual disability. Am J Med Genet Part A 155: 2838–2840.
New case of Primrose syndrome with mild intellectual disability†
Version of Record online: 9 SEP 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 11, pages 2838–2840, November 2011
How to Cite
Posmyk, R., Leśniewicz, R., Chorąży, M. and Wołczyński, S. (2011), New case of Primrose syndrome with mild intellectual disability. Am. J. Med. Genet., 155: 2838–2840. doi: 10.1002/ajmg.a.34257
- Issue online: 20 OCT 2011
- Version of Record online: 9 SEP 2011
- Manuscript Accepted: 18 JUL 2011
- Manuscript Received: 16 FEB 2011
- Primrose syndrome;
- ossification of ear cartilage;
- progressive wasting of the distal muscles;
- hypergonadotropic hypogonadism
We report on a 27-year-old man, who represents the sixth and the youngest published case of Primrose syndrome. Primrose syndrome (PS) (OMIM#295090) is an extremely rare entity of unknown etiology characterized by the progressive wasting of distal muscles of the legs, the small muscles of the hands resulting in contractures, the presence of intellectual disability, hearing problems, cataracts, brain calcification, and the ossification of ear cartilage. All the main manifestations were present in our patient. Despite the phenotypic similarity to five other cases, our patient had mild intellectual disability. Additionally we found hypergonadotropic hypogonadism and a low bone density due to progressive osteoporosis. We discuss our observations in relation to previously published cases, and we stress the need for the detail and phenotypic descriptions of further cases as PS remains rare, and the genetic basis is still undiscovered. © 2011 Wiley Periodicals, Inc.