• Title of article

    A 3.5 year-old Boy with FTT and Skin Lesions

  • Author/Authors

    Hooman, Nakysa Consultant Pediatric Nephrology - Ali-asghar children hospital, Iran University of Medical Sciences , Dehgan, Marzieh

  • Pages
    4
  • From page
    1
  • To page
    4
  • Abstract
    Fanconi anemia is a rare disease associated with hematologic abnormality and congenital anomalies. The majority of patients with Fanconi anemia have birth defects, such as altered skin pigmentation, short stature, thumb or thumb and radial anomalies, abnormal male gonads, microcephaly, eye anomalies, structural renal defects, abnormal ears or hearing , or developmental delay. Asymptomatic siblings need to be screened for occult Fanconi anemia. Pancytopenia can cure by stem cell transplantation. Treatment is recommended for signi
  • Keywords
    A 3.5 year-old Boy , FTT , Skin Lesions
  • Journal title
    Astroparticle Physics
  • Serial Year
    2016
  • Record number

    2451701