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Anais Brasileiros de Dermatologia

Volumn 81, Issue 5, 2006, Pages 487-489

  Ottoni, Fernanda Assis ^a,b   Pimenta, Mariana Rodrigues ^a   Froes, Giselle Carvalho ^a   Do Vale, Everton Carlos Siviero ^a  

^a FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^b NONE   (Brazil)

Author keywords

Adult; Chromosome breakage; Fanconi anemia; Hyperpigmentation; Leukopenia; Macrocytic anemia

Indexed keywords

ADULT; ANAMNESIS; CASE REPORT; CLINICAL FEATURE; CONFERENCE PAPER; FANCONI ANEMIA; HUMAN; HYPERPIGMENTATION; LABORATORY TEST; MALE; PROGNOSIS; SKIN DISEASE;

EID: 34248636999     PISSN: 03650596     EISSN: 18064841     Source Type: Journal    
DOI: 10.1590/s0365-05962006000500013     Document Type: Conference Paper

References (6)

1. Bluhen SS, Anstey AV. Disorders of skin colour. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook's Texbook of Dermatology. Malde: Blackwell; 2004. p.39.1-68.
2. Tischkowitz M, Dokal I. Fanconi anaemia and leukaemia - clinical and molecular aspects. Br J Haematol. 2004;126:176-91.
3. Dosik H, Hsu LY, Tadaro GL, Lee SL, Hirschhorn K, Selirio ES, et al. Leukemia in Fanconi's anemia: cytogenetic and tumor vírus susceptibility studies. Blood. 1970;36:341-52.
4. Kenneth HK. Heritable Diseases with increased sensitivity of celular injury. In: Freedberg IM, Eizen AZ, Wolff K, Austen KF, Goldsmith LA, Katz S, editors. Fitzpatrick's Dermatology in General Medicine. New York: McGraw-Hill; 2003. p.1508-21.
5. Tsao H. Neurofibromatosis and tuberous sclerosis. In: Bolognia JL, Horn TD, Mascaro JM, Mancini AJ, Salasche SJ, Saurat JH eds, et al. Dermatology. London: Mosby; 2003. p. 853-67.
6. Farrell GC. Fanconi's familial hypoplastic anaemia with some unusual features. Med J Aust. 1976;1:116-8.