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Kindler syndrome: report of two cases.
[kindler syndrome]
Kindler
syndrome
is
a
rare
autosomal
recessive
genodermatosis
characterized
by
trauma-induced
blisters
,
progressive
poikiloderma
and
varying
degrees
of
photosensitivity
.
In
2003
,
loss
-of-function
mutations
were
identified
in
the
gene
KIND
1
mapped
to
chromosome
20
p
12
.
3
.
In
this
paper
,
we
report
Kindler
syndrome
in
two
children
born
to
consanguineous
parents
presenting
acral
blistering
,
photosensitivity
,
poikiloderma
,
cutaneous
atrophy
and
periodontitis
.