Rare Diseases Symptoms Automatic Extraction
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A random Abstract
Our Project
Our Team
Genetic testing by cancer site: skin.
[cowden syndrome]
Many
hereditary
cancer
predisposition
syndromes
are
associated
with
cutaneous
findings
,
both
benign
and
malignant
.
Dermatological
examination
and
histopathology
,
when
combined
with
a
thorough
personal
and
family
medical
history
,
play
an
important
role
in
the
diagnosis
of
cancer
predisposition
syndromes
.
Skin
findings
are
an
important
diagnostic
tool
for
a
variety
of
cancer
syndromes
,
including
Cowden
syndrome
,
Birt-
Hogg-
Dubé
,
hereditary
leiomyomatosis
renal
cell
carcinoma
,
and
others
.
This
article
focuses
on
the
phenotype
,
medical
management
,
and
genetic
testing
for
4
hereditary
cancer
syndromes
that
include
cutaneous
findings
:
hereditary
melanoma
,
basal
cell
nevus
syndrome
,
neurofibromatosis
type
1
,
and
neurofibromatosis
type
2
.
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