Volume : V, Issue : V, May - 2016

A Case study of Rare case of Fanconi anemia

Dr Anil J Katara, Dr Dushyant B Barot

Abstract :

 FA is a rare autosomal recessive disease characterized by congenital abnormalities, defective haematopoisis and a high risk of developing acute myeloid leukemia, myelodysplastic syndrome and cancers. Diagnosis is based on morphological abnormalities, haematological abnormalities and genetic tests. We report a case of FA in a 3 and ½ year old female child presenting with pallor and pancytopenia.

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Article: Download PDF   DOI : 10.36106/ijsr  

Cite This Article:

Dr Anil J Katara, Dr Dushyant B Barot A Case study of Rare case of Fanconi anemia International Journal of Scientific Research, Vol : 5, Issue : 5 MAY 2016

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