-
Figure of
various morbidities ****ociated with
neurofibromatosis type II. The
three types of
neurofibromatosis are
caused by
different mutations on chromosomes...
-
Neurofibromatosis type I (NF-1), or von
Recklinghausen syndrome, is a
complex multi-system
neurocutaneous disorder caused by a
subset of
genetic mutations...
-
Neurofibromatosis type II (also
known as
MISME syndrome –
multiple inherited schwannomas, meningiomas, and ependymomas) is a
genetic condition that may...
- as
neurofibromatosis type 1 and McCune–Albright syndrome. The size and
shape of the
spots can vary in
terms of description. In
neurofibromatosis type...
-
cases are
diagnosed in
people with
neurofibromatosis; the
lifetime risk for an
MPNST in
patients with
neurofibromatosis type 1 is 8–13%.
MPNST with rhabdomyoblastomatous...
- gene, the same gene ****ociated with
neurofibromatosis type 1. It is
believed that
Watson syndrome and
neurofibromatosis-1
result from
allelic mutations at...
-
often mistaken for
neurofibromatosis type I. It is
caused by
mutations in the SPRED1 gene. It is also
known as
neurofibromatosis type 1-like syndrome...
- (depending on the
specific allele expressed) such as
Watson syndrome and
neurofibromatosis type 1 (NF1, also
known as von
Recklinghausen syndrome). Symptoms...
- is
considered to be the
hallmark and main
diagnostic criterion of
Neurofibromatosis Type II (NF2), a
genetic disorder that is heritable, progressive,...
- this type of
disorder are Huntington's disease,: 58
neurofibromatosis type 1,
neurofibromatosis type 2,
Marfan syndrome,
hereditary nonpolyposis colorectal...
