Three siblings with a lifelong history of a bleeding disorder and thrombocytopenia died from a myeloproliferative disease. In 2, the terminal event resembled juvenile chronic myelogenous leukemia, and in the third, the diagnosis was acute monocytic leukemia. A family study revealed that the mother a
✦ LIBER ✦
Neutrophil dysfunction in a family with a SAPHO syndrome–like phenotype
✍ Scribed by Polly J. Ferguson; Mary A. Lokuta; Hatem I. El-Shanti; Leah Muhle; Xinyu Bing; Anna Huttenlocher
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 122 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A fatal myeloproliferative syndrome in a
✍
Ruth E. Luddy; Lorraine A. A. Champion; Allen D. Schwartz
📂
Article
📅
1978
🏛
John Wiley and Sons
🌐
English
⚖ 661 KB
New phenotypic aspects in a family with
✍
G. Cristofaro; H. T. Lynch; M. L. Caruso; A. Attolini; G. Dimatteo; P. Giorgio;
📂
Article
📅
1987
🏛
John Wiley and Sons
🌐
English
⚖ 704 KB
Robinow syndrome: Phenotypic variability
✍
Nicola Brunetti-Pierri; Daniela del Gaudio; Hartmut Peters; Henri Justino; Claus
📂
Article
📅
2008
🏛
John Wiley and Sons
🌐
English
⚖ 365 KB
👁 2 views
Premature adrenal cortical dysfunction i
✍
Ng, David ;Stratakis, Constantine A.
📂
Article
📅
2000
🏛
John Wiley and Sons
🌐
English
⚖ 57 KB
Neutrophil elastase in patients with hom
✍
Samarkos, M.; Aessopos, A.; Fragodimitri, C.; Karagiorga, M.; Kalotychou, V.; Vo
📂
Article
📅
2000
🏛
John Wiley and Sons
🌐
English
⚖ 44 KB
In this study we investigated the possible role of neutrophil (PMN) elastase and its natural inhibitor, ␣1-proteinase inhibitor (␣1-PI) in the pathogenesis of the pseudoxanthoma elasticum (PXE)-like syndrome which is found in patients with homozygous -thalassemia. We studied 30 -thalassemia homozy
Crane-Heise syndrome: A second familial
✍
Zand, Dina J. ;Carpentieri, David ;Huff, Dale ;Medne, Livija ;Napierala, Dobrawa
📂
Article
📅
2003
🏛
John Wiley and Sons
🌐
English
⚖ 259 KB
👁 3 views