P27.9 A case of pontocerebellar hypoplasia associated with nevoid hyperpigmentation and dysmorphic findings
β Scribed by F.M. Sonmez; S. Yayli; S. Kul; F. Celep; A.K. Ozkaya
- Book ID
- 114360736
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 43 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1090-3798
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract We report a case of a 23βyearβold pregnant woman, who underwent amniocentesis after ultrasound (US) examination in the first trimester which revealed a nuchal translucency thickness of 2.9 mm. Cytogenetic analysis revealed complete tetrasomy of the short arm of chromosome 9. Further US
## Abstract Polyneuropathy, organomegaly, endocrinopathy, M protein and skin changes (POEMS) syndrome is a rare multiβsystem disease. We describe the ultrasonography (US) and color Doppler ultrasonography (CDUS) findings of peripheral neuropathy in a patient with POEMS syndrome. In US examination,
We report a 44-year-old female with Isaacs' syndrome, peripheral motor neuropathy, and features of central pontine myelinolysis (CPM). The patient presented with stiffness and muscle spasms accompanied by profound sweating. She also had bilateral Babinski signs. Electrodiagnostic abnormalities were