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Volumn 334, Issue 3, 2007, Pages 206-208

Dyskeratosis congenita associated with hypocellular myelodysplastic syndrome: A case report

Author keywords

Dyskeratosis congenita; Myelodysplastic syndrome

Indexed keywords

ADOLESCENT; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DYSKERATOSIS CONGENITA; FAMILY HISTORY; FEMALE; HUMAN; HUMAN TISSUE; LABORATORY TEST; MYELODYSPLASTIC SYNDROME; PHYSICAL EXAMINATION; SKIN EXAMINATION;

EID: 34548671424     PISSN: 00029629     EISSN: None     Source Type: Journal    
DOI: 10.1097/MAJ.0b013e3181405e51     Document Type: Article
Times cited : (1)

References (13)
  • 1
    • 0000605996 scopus 로고
    • Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris (poikiloderma atrophicans vascularis Jacobi)
    • Zinsser F. Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris (poikiloderma atrophicans vascularis Jacobi). Ikonogr Derm (Kyoto) fas 1906;5:219-223.
    • (1906) Ikonogr Derm (Kyoto) fas , vol.5 , pp. 219-223
    • Zinsser, F.1
  • 2
    • 0000757535 scopus 로고
    • A unique case of reticular pigmentation of the skin with atrophy
    • Engman M. A unique case of reticular pigmentation of the skin with atrophy. Arch Derm Syph Suppl 1926;13:685-687.
    • (1926) Arch Derm Syph Suppl , vol.13 , pp. 685-687
    • Engman, M.1
  • 3
    • 0002924576 scopus 로고
    • Dyskeratosis congenita with pigmentation, dystrophia unguis and leukokeratosis oris
    • Cole H, Rauschkolb J, Toomey J. Dyskeratosis congenita with pigmentation, dystrophia unguis and leukokeratosis oris. Arch Derm Syph 1930;21:71-95.
    • (1930) Arch Derm Syph , vol.21 , pp. 71-95
    • Cole, H.1    Rauschkolb, J.2    Toomey, J.3
  • 5
    • 0242354776 scopus 로고    scopus 로고
    • Dyskeratosis congenita: Its link to telomerase and aplastic anaemia
    • Dokal I, Vulliamy T. Dyskeratosis congenita: its link to telomerase and aplastic anaemia. Blood Rev 2003;17:217-225.
    • (2003) Blood Rev , vol.17 , pp. 217-225
    • Dokal, I.1    Vulliamy, T.2
  • 6
    • 0031755117 scopus 로고    scopus 로고
    • Dyskeratosis congenita: Multisystemic disorder with special consideration of immunologic aspects: a review of the literature
    • Solder B, Weiss M, Jager A, et al. Dyskeratosis congenita: multisystemic disorder with special consideration of immunologic aspects: a review of the literature. Clin Pediatr (Phila) 1998;37;521-530.
    • (1998) Clin Pediatr (Phila) , vol.37 , pp. 521-530
    • Solder, B.1    Weiss, M.2    Jager, A.3
  • 7
    • 0037362432 scopus 로고    scopus 로고
    • Human genome and diseases: Review dyskeratosis congenita
    • Marrone A, Mason PJ. Human genome and diseases: review dyskeratosis congenita. Cell Mol Life Sci 2003;60;507-517.
    • (2003) Cell Mol Life Sci , vol.60 , pp. 507-517
    • Marrone, A.1    Mason, P.J.2
  • 8
    • 0032424906 scopus 로고    scopus 로고
    • Dyskeratosis congenita (DC) registry: Identification of new features of DC
    • Knight S, Vulliamy T, Copplestone A, et al. Dyskeratosis congenita (DC) registry: identification of new features of DC. Br J Haematol 1998;103:990-996.
    • (1998) Br J Haematol , vol.103 , pp. 990-996
    • Knight, S.1    Vulliamy, T.2    Copplestone, A.3
  • 9
    • 0033754823 scopus 로고    scopus 로고
    • Dyskeratosis congenita in all its forms
    • Dokal I. Dyskeratosis congenita in all its forms. Br J Haematol 2000;110:768-779.
    • (2000) Br J Haematol , vol.110 , pp. 768-779
    • Dokal, I.1
  • 10
    • 20344403331 scopus 로고    scopus 로고
    • Lack of mutations of the human telomerase RNA gene (hTERC) in myelodysplastic syndrome
    • Ohyashiki K, Shay JW, Ohyashiki JH. Lack of mutations of the human telomerase RNA gene (hTERC) in myelodysplastic syndrome. Haematologica 2005;90:691.
    • (2005) Haematologica , vol.90 , pp. 691
    • Ohyashiki, K.1    Shay, J.W.2    Ohyashiki, J.H.3
  • 11
    • 33746374390 scopus 로고    scopus 로고
    • Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome
    • Field JJ, Mason PJ, An P, et al. Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome. J Pediatr Hematol Oncol 2006;28:450-453.
    • (2006) J Pediatr Hematol Oncol , vol.28 , pp. 450-453
    • Field, J.J.1    Mason, P.J.2    An, P.3
  • 12
    • 33744472191 scopus 로고    scopus 로고
    • TERC mutations in children with refractory cytopenia
    • Ortmann CA, Niemeyer CM, Wawer A, et al. TERC mutations in children with refractory cytopenia. Haematologica 2006;91:707-708.
    • (2006) Haematologica , vol.91 , pp. 707-708
    • Ortmann, C.A.1    Niemeyer, C.M.2    Wawer, A.3
  • 13
    • 0041592752 scopus 로고    scopus 로고
    • Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
    • Yamaguchi H, Baerlocher GM, Lansdorp PM, et al. Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. Blood 2003 102:916-918.
    • (2003) Blood , vol.102 , pp. 916-918
    • Yamaguchi, H.1    Baerlocher, G.M.2    Lansdorp, P.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.