Rare Diseases Symptoms Automatic Extraction
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A random Abstract
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Recent advances in the study of somatic mosaicism and diseases other than cancer.
[proteus syndrome]
Somatic
mosaicism
is
well
appreciated
as
a
cause
of
cancer
and
,
possibly
,
aging
.
Somatic
mosaicism
as
the
cause
of
other
diseases
is
becoming
more
appreciated
.
It
is
especially
important
in
the
causation
of
deforming
diseases
(
e
.
g
.
,
Proteus
syndrome
;
Sturge-
Weber
syndrome
)
which
are
not
inherited
because
early
developmental
expression
is
lethal
.
It
also
known
to
make
an
important
contribution
to
neurological
,
dermatological
,
hematological
and
other
diseases
(
and
probably
all
diseases
but
many
in
which
it
is
harder
to
detect
)
.
There
have
been
exciting
recent
advances
in
the
detection
of
somatic
mosaicism
.
In
particular
,
for
many
diseases
of
somatic
overgrowth
in
which
somatic
mosaicism
as
the
sole
cause
was
predicted
,
the
gene
somatically
mutated
has
been
found
.
A
limited
number
of
pathways
seem
involved
in
these
disorders
,
some
of
which
are
also
implicated
in
cancer
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated