- A Case of Weill-Marchesani Syndrome with Inversion of Chromosome 15
-
Chung JL, Kim SW, Kim JH, Kim TI, Lee HK, Kim EK
- KMID: 754646
- Korean J Ophthalmol.
- 2007 Dec;21(4):255-260.
- doi: 10.3341/kjo.2007.21.4.255
PURPOSE: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to anterior dislocation of a spherophakic lens and corneolenticular contact. METHODS: A 17-year-old woman presented... -
- CITED
-
- Close
- SHARE
-
- Close
- Hematologic and Clinical Features of 3q21q26 Syndrome: Extremely Poor Prognosis and Association with Central Diabetes Insipidus
-
Chung HJ, Seo EJ, Kim KH, Jang S, Park CJ, Chi HS, Lee JH, Lee JH, Lee KH
- KMID: 1781473
- Korean J Lab Med.
- 2007 Apr;27(2):133-138.
- doi: 10.3343/kjlm.2007.27.2.133
BACKGROUND: 3q21q26 syndrome includes chromosomal abnormalities of inv(3)(q21q26), t(3;3) (q21;q26), and ins(3;3)(q26;q21q26). It causes hematological diseases by the leukemogenic mechanism that the enhancer of ribophorin I gene in 3q21... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Therapy-related Acute Myeloid Leukemia associated with inv(16)
-
Lee SY, Kim M, Lim J, Kim Y, Han K, Kim SY, Kim HJ, Park IY
- KMID: 1121654
- Korean J Lab Med.
- 2007 Feb;27(1):19-21.
- doi: 10.3343/kjlm.2007.27.1.19
The inv(16)(p13q22) is found in de novo AML and is closely associated with the FAB subtype M4eo. The inv(16) is rarely reported in therapy-related AML (t-AML) patients. Herein, we report... -
- CITED
-
- Close
- SHARE
-
- Close
