Rare Diseases Symptoms Automatic Extraction
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Hereditary nonmelanoma skin cancer.
[oculocutaneous albinism]
Cutaneous
basal
and
squamous
cell
carcinomas
are
among
the
most
frequent
malignancies
in
the
white
population
,
with
the
annual
incidence
estimates
ranging
from
1
million
to
3
.
5
million
cases
in
the
United
States
.
These
tumors
can
occur
either
sporadically
or
in
the
context
of
hereditary
genodermatoses
with
cancer
predisposition
,
such
as
basal
cell
nevus
syndrome
,
xeroderma
pigmentosum
,
epidermolysis
bullosa
,
or
oculocutaneous
albinism
.
Different
genes
and
signaling
pathways
have
been
shown
to
play
a
central
role
in
the
development
and
growth
of
these
tumors
.
This
article
overviews
the
clinical
features
,
diagnostic
criteria
,
and
the
most
recent
data
on
genetic
routes
of
the
major
hereditary
syndromes
predisposed
to
the
development
of
nonmelanoma
skin
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