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A total of 18 patients within the age range of 5-13 years, 12 male and 6 female, are diagnosed as having Fanconi's aplastic anemia on the basis of congenital abnormalities, pancytopenia, bone marrow hypoplasia, and chromosomal and hematologic analysis. The hereditary and familial basis of Fanconi's aplastic anemia was apparent in this series. Common abnormalities were growth retardation, café au lait spots, hyperpigmentations, microcephaly, phalange deformities, mental retardation, and hypogenitalism; chromosome abnormalities were detected in the majority of our cases. Mast cells were observed in the bone marrow in most of the patients. 1 case developed acute myelomonocytic leukemia.
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
July 1999,
Indian pediatrics,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
September 2000,
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S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
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S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
September 1979,
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S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
October 1975,
Voprosy okhrany materinstva i detstva,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
January 1985,
Pediatria polska,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
December 1964,
Zeitschrift fur Kinderheilkunde,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
November 1996,
Current opinion in hematology,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
January 1953,
La Pediatria,
S Gözdaşoğlu, and
A O Cavdar, and
A Arcasoy, and
E Babacan, and
O Sanal
January 1953,
Zdravstveni vestnik,
