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
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