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Fanconi anemia (FA) is a rare,
autosomal recessive,
genetic disease resulting in
impaired response to DNA
damage in the FA/BRCA pathway.
Although it is...
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Fanconi syndrome or
Fanconi's syndrome (English: /fɑːnˈkoʊni/, /fæn-/) is a
syndrome of
inadequate reabsorption in the
proximal renal tubules of the kidney...
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Fanconi may
refer to:
Fanconi anemia, a
genetic disease Fanconi syndrome, a
kidney disease Guido Fanconi (1892–1979), a
Swiss pediatrician This disambiguation...
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urologic (incontinence,
Fanconi syndrome,
chronic kidney failure 13%),
behavior ("unspecified" and
aggression 9%), and
cancer (9%).
Fanconi syndrome, an inheritable...
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Fanconi anemia,
complementation group E
protein is a
protein that in
humans is
encoded by the
FANCE gene. The
Fanconi anemia complementation group (FANC)...
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Fanconi–Bickel
syndrome is a form of
glycogen storage disease named for
Guido Fanconi and
Horst Bickel, who
first described it in 1949. It is ****ociated...
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Fanconi anaemia,
complementation group A, also
known as FAA, FACA and FANCA, is a
protein which in
humans is
encoded by the
FANCA gene. It
belongs to...
- to a
sibling that is
affected with a
fatal disease, such as
cancer or
Fanconi anemia, that can best be
treated by
hematopoietic stem cell transplantation...
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Guido Fanconi (English: /fɑːnˈkoʊni/) (1
January 1892 – 10
October 1979) was a
Swiss pediatrician.
Fanconi was born on 1
January 1892 in Poschiavo, a small...
- PALB2 (also
known as FANCN),
similar to
biallelic BRCA2 mutations,
cause Fanconi anemia.
Mutations in this gene have been ****ociated with an
increased risk...
