Development of 5q- myelodysplasia in a patient with sarcoidosis
β Scribed by Allan R. Tunkel; Kenneth J. Sebastianelli; Niraj Pandit; Jerome I. Brody
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 311 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The Nager syndrome is the most common form of acrofacial dysostosis. Although autosomal dominant and recessive forms of acrofacial dysostosis have been described the molecular etiology of these disorders is unknown. We report on a child with acrofacial dysostosis, critical aortic stenosis, and a del
A patient with Philadelphia-positive (Ph+) chronic myelogenous leukemia (CML) was diagnosed with cutaneous sarcoidosis after treatment with interferon-alpha (IFN-β£). Following IFN-β£ dose reduction, the skin lesions disappeared. Few cases of sarcoidosis associated with IFN treatment have been reporte