- A Case of dyskeratosis congenita
-
No authors listed
- KMID: 2038927
- Korean J Dermatol.
- 1990 Apr;28(2):231-235.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Dyskeratosis Congenita in a Woman
-
Kim CY, Kim TH, Yoon TJ
- KMID: 2303157
- Korean J Dermatol.
- 2001 Oct;39(10):1162-1165.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A case of dyskeratosis congenita
-
Han JW, Bae JW, Choi WG, Kim HK, Lee KS
- KMID: 2252496
- Korean J Hematol.
- 1991 Oct;26(2):425-428.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Dyskeratosis Congenita
-
Kim DH, Kang HA, Park HJ, Kim CW, Kim HO
- KMID: 2163948
- Ann Dermatol.
- 2000 Mar;12(1):56-59.
- doi: 10.5021/ad.2000.12.1.56
Dyskeratosis congenita is a rare genodermatosis of ectodermal dysplasia, which is characterized by the diagnostic triad consisting of reticulated hyperpigmentation, dystrophic nails, and leukoplakia. There is a predisposition to malignancy,... -
- CITED
-
- Close
- SHARE
-
- Close
- Interstitial Lung Disease in a Patient with Dyskeratosis Congenita
-
Kim HJ, Kim KJ, Lee KH, Shin KC, Chung JH, Hyun MS, Kim KH
- KMID: 2320253
- Tuberc Respir Dis.
- 2013 Feb;74(2):70-73.
Dyskeratosis congenita is a rare congenital disorder characterized by a triad of reticular pigmentation of the skin, dystrophic nails, and leukoplakia of the mucous membrane. Sometimes it is associated with... -
- CITED
-
- Close
- SHARE
-
- Close
- Dyskeratosis Congenita
-
Oh S, Kim BD, Lee DH, Lee KH
- KMID: 1619903
- Korean J Dermatol.
- 2003 Mar;41(3):377-380.
Dyskeratosis congenita is a rare multisystemic genodermatosis of ectodermal dysplasia, and is characterized by the diagnostic triad consisting of reticulated hyperpigmentation, dystrophic nails, and leukoplakia. Complications such a malignancy and... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Dyskeratosis Congenita
-
Choi DY, Koh CJ
- KMID: 2085655
- Korean J Dermatol.
- 1988 Oct;26(5):739-743.
Dyskeratosis congsnita is a rare congenital disorder characterized by the triad of reticular pigmentation of the skin. dystrophic naila, and leukoplakia of the mucous membrane, and is often associated with... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Dyskeratosis Congenita with Myelodysplastic Syndrome
-
Shin HJ, Poo CS, Kim JS, Bae WH, Hong JH, Chung JS, Lee EY, Cho GJ
- KMID: 1533978
- Korean J Hematol.
- 1999 Nov;34(4):614-618.
Dyskeratosis congenita is a rare form of ectodermal dysplasia consisting of dystrophic nails, reticular hyperpigmentation and leukoplakia, that is often associated with aplastic anemia. We have experienced a 17 year-old-man... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Familial Telangiectasia of Face
-
Ahn SY, Suh SB
- KMID: 1664743
- Korean J Dermatol.
- 1977 Dec;15(4):459-463.
A case of familial telangiectasia of face resembling lupus erythematosus but no having other involved symptoms, except ichthyosis vulgaris of lower legs in all 4 sisters, appeared on 8 months... -
- CITED
-
- Close
- SHARE
-
- Close
- Dyskeratosis Congenita in a Girl
-
Yi JS, Kook H, Paik HJ, Kim SY, Choi IS, Kim SJ, Sohn KR, Nam HS, Hwang TJ
- KMID: 2278307
- Korean J Pediatr Hematol Oncol.
- 2003 Oct;10(2):293-298.
Dyskeratosis congenita (DC) is a rare genetic disorder encompassing abnormal skin pigmentation, dystrophic nails, leukoplakia of mucous membranes and others. Bone marrow failure is the cause of early mortality. Moreover,... -
- CITED
-
- Close
- SHARE
-
- Close
- Current insights into inherited bone marrow failure syndromes
-
Chung NG, Kim M
- KMID: 2353160
- Korean J Pediatr.
- 2014 Aug;57(8):337-344.
Inherited bone marrow failure syndrome (IBMFS) encompasses a heterogeneous and complex group of genetic disorders characterized by physical malformations, insufficient blood cell production, and increased risk of malignancies. They often... -
- CITED
-
- Close
- SHARE
-
- Close
- The Frequency of Glycophosphatidyl Inositol-Anchored Protein-Negative Paroxysmal Nocturnal Hemoglobinuria Cells in Pediatric Aplastic Anemia Analyzed by Flow Cytometry
-
Kim SJ, Kook H, Cho D, Kim SY, Noh HY, Choi IS, Lee JS, Ryang DW, Hwang TJ
- KMID: 2278261
- Korean J Pediatr Hematol Oncol.
- 2003 Apr;10(1):39-48.
PURPOSE: Paroxysmal nocturnal hemoglobinuria (PNH) has been known to be a late clonal complication of aplastic anemia (AA). Flow cytometric analysis using CD55 and CD59 antibodies became the gold standard... -
- CITED
-
- Close
- SHARE
-
- Close
