-
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
human disorder caused by the
mutation of
neurofibromin 1 (NF-1)...
-
Neurofibromatosis type II (also
known as
MISME syndrome –
multiple inherited schwannomas, meningiomas, and ependymomas) is a
genetic condition that may...
-
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...
-
Neurofibromatosis type 4 (also
known as "
Neurofibromatosis variant type")
resembles von Recklinghausen's disease, but also
presents with
cutaneous neurofibromas...
- is
considered to be the
hallmark and main
diagnostic criterion of
Neurofibromatosis Type II (NF2), a
genetic disorder that is heritable, progressive,...
- Lane), a
computer analyst, and
later vice
president of
Neurofibromatosis Inc., the
neurofibromatosis support group of West Michigan, and
Homer Edward "Ed"...
-
neurofibromatosis type 1.
Epilepsy is seen in 4-7% of patients.
Musculoskeletal system manifestations can
develop in
patients with
neurofibromatosis type...
- as
neurofibromatosis type 1 and McCune–Albright syndrome. The size and
shape of the
spots can vary in
terms of description. In
neurofibromatosis type...
- and campaigner. He
appeared in the 2013 film
Under the Skin. He has
neurofibromatosis and has been
involved in
outreach programmes to
prevent bullying ****ociated...
