Abstract
A case is described of Fanconi's anaemia in a girl who suffered from dwarfism due to congenital hypoplasia of the pituitary and from other congenital malformations. The pancytopenia manifested itself at the age of 2 years and was resistant to a combined corticosteroid-testosterone treatment. Unusual findings in this case were congenital hydrocephalus, hypoplastic spleen, and hypoplasia of thyroid together with persistently high PBI serum levels but without apparent changes in thyroid function.
Cite
CITATION STYLE
London, R., Drukker, A., & Sandbank, U. (1965). Fanconi’s anaemia with hydrocephalus and thyroid abnormality. Archives of Disease in Childhood, 40(209), 89–92. https://doi.org/10.1136/adc.40.209.89
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