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Periodontal diseases in children and adolescents: a clinician's perspective part 2.
[cohen syndrome]
The
general
dental
practitioner
and
paediatric
dentist
are
in
a
unique
position
to
identify
and
distinguish
between
a
seemingly
innocuous
condition
that
may
be
a
normal
physiological
aberration
or
an
early
sign
of
severe
destructive
periodontal
disease
.
Although
severe
destructive
periodontal
conditions
are
uncommon
in
children
,
it
is
essential
that
children
receive
a
periodontal
screening
as
part
of
their
regular
dental
examination
.
Early
diagnosis
ensures
a
high
likelihood
of
a
successful
therapeutic
outcome
,
primarily
by
reduction
of
aetiologic
factors
,
remedial
therapy
and
development
of
an
effective
maintenance
protocol
.
This
prevents
the
recurrence
and
progression
of
disease
and
reduces
the
incidence
of
tooth
loss
.
In
the
first
article
,
we
discussed
the
classification
,
plaque-induced
and
non
plaque-induced
gingival
diseases
,
localized
and
generalized
forms
of
chronic
as
well
as
aggressive
periodontitis
.
In
this
second
article
,
we
discuss
periodontitis
as
a
manifestation
of
systemic
disease
,
necrotizing
periodontal
diseases
,
periodontal
screening
and
basic
periodontal
examination
,
and
treatment
of
periodontal
diseases
in
children
and
adolescents
.
Incorporation
of
periodontal
screening
in
regular
dental
examination
by
dentists
can
help
in
early
diagnosis
and
treatment
of
periodontal
diseases
.
This
could
prevent
further
progression
of
disease
and
reduce
the
frequency
of
tooth
loss
.
Diseases
Validation
Diseases presenting
"early diagnosis"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
cystinuria
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
hirschsprung disease
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kabuki syndrome
kallmann syndrome
kindler syndrome
krabbe disease
locked-in syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
triple a syndrome
typhoid
von hippel-lindau disease
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
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