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
Fraser syndrome (cryptophthalmos-syndactyly syndrome): A review of eleven cases with postmortem findings
β Scribed by Boyd, P. A. ;Keeling, J. W. ;Lindenbaum, R. H. ;Neri, Giovanni ;Reynolds, James F.
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 485 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Myelodysplastic syndrome (MDS) with erythroid hypoplasia/aplasia has not yet been clearly defined, and in most patients it is mistaken for acquired pure red cell aplasia (PRCA). We report a patient with severe transfusion-dependent anemia (Hb 6.9 g/dl) and reticulocytopenia. WBC and platelet counts
## Abstract IMAGe syndrome is a rare condition, first reported by Vilain et al., in 1999, characterized by __i__ntrauterine growth restriction, __m__etaphyseal dysplasia, congenital __a__drenal hypoplasia, and __g__enital anomalies. Patients with this condition may present shortly after birth with