Documente Academic
Documente Profesional
Documente Cultură
DISEASES IN
CHILDREN
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INTRODUCTION
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Periodontitis
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[E] Systemic disease forms
Leukocyte disorders
Neutropenia
Chediak-Higashi syndrome
Leucocyte adhesion deficiency syndrome
Papillon-Lefevre syndrome
Down syndrome
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Diabetes mellitus
Hypophosphatasia
Histiocytosis X
Ehlers-Danlers syndrome
Juvenile hyaline fibromatosis of gingiva
Acquired immunodeficiency syndrome
Virus-associated hemophagocytic syndrome
Malnutrition
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CLASSIFICATION OF
PERIODONTAL DISEASE
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[A] Adult onset periodontitis
Hypophosphatasia
Leucocyte adhesion defect
Papillon-lefevre syndrome
Down syndrome
Chediak-Higashi syndrome
Langerhans cell histiocytosis
Acute leukemia
Insulin-dependent diabetes mellitus
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[D] Drug induced gingival overgrowth
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PERIODONTAL
DISEASES &
CONDITIONS
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PREPUBERTAL
PERIODONTITIS
Localized
Generalized
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LOCALIZED PREPUBERTAL
PERIODONTITIS
Clinical features
Onset at about 4 years of age in
healthy children
Rapid bone loss at the affected sites
Etiology
Functional abnormalities in neutrophils
or monocytes but not both
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Affected site harbours actinobacillus
actinomycetemcomitan, prevotella intermedia
& porphyromonous gingivalis
Treatment
Local debridement
Antibiotic therapy
Improved oral hygiene
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GENERALISED
PREPUBERTAL
PERIODONTITIS
Clinical features
Occurs in children with persistent
infection & delayed wound healing
Alveolar bone destruction is more rapid
Etiology
Functional abnormalities occur in both
neutrophils & monocytes
The generalized type has been associated
with leukocyte adhesion deficiency
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TREATMENT
Antibiotic therapy
Extraction of affected teeth
SEQUELAE
ALISED TYPE
appears to be self limiting & affects mainly permanent first molars
cisors in adolescents
one loss is rapid & is not commensurate with amount of local
ants present such as plaque & calculus
OLOGY
usceptible individuals has both functional defects involving
utrophils & high virulent strains of actinobacillus actinomycetem-
mitans & bacteriodes species
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TREAMENT
--Self limiting
--No treatment required
NICAL FEATURES
More common in young adults involving permanent
ntition
ccurs in presence of marked gingival inflammation & gross plaque
cumulation
TIOLOGY:-
Subgingival plaque from affected site harbours high percentage
Of porphyromonas gingivalis
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TREATMENT
Medical debridment
-- Antiobiotic therapy
TETRACYCLINE 1gm/day FOR 14 TO 21 DAYS
OR
AMOXICILLIN 1gm/day + METRONIDAZOLE
750mgm/day FOR 7 DAYS
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SYSTEMIC DISORDERS
ASSOCIATED
WITH PERIODONTAL DISEASES
LEUKAEMIA:- This neoplastic disorder results in
abnormal & uncontrolled proliferation of immature leukocyte
ORAL MANIFESTATION:-
(i) Gingival enlargement with ulceration
(ii) Thinning of lamina dura
(iii)Destruction of periodontal ligament
(iv)Tooth migration
ORAL MANIFESTATION
(i) Alveolar bone loss around primary level
(ii) Severe ulcerative gingivitis
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CYCLIC NEUTROPENIA
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HYPOPHOSPHATASIA:- It is characterised
by low serum alkaline phosphatase & reciprocal
change in urine phosphoethanol amine level
ORAL MANIFESTATION:-
(i) Premature mobility & loss of primary teeth
[Incisors are affected more than molars]
(iI) Acementogenesis
(iii) Dentinal dysplasia
(Iv) Enlarged pulp chamber
ORAL MANIFESTATION:-
(i) Premature loss of both primary & permanent teeth
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HISTOCYTOSIS X
It is non lipidreticuloendotheliosis marked
by multiple hard & soft tissue lesions
containing
histocytes & eosinophils
ORALMANI
ACRODYNIA
t is also called pinks or swifts diseases
ETIOLOGY
Due to excessive exposure to merqury
ORAL MANIFESTATION
(i) Glossitis
(ii) Premature erruption
(iii) Exfoliation of teeth www.FourthMolar.com
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DIABETES MELLITUS &
CHRONIC GRANULOMATOUS
DISEASES
DOWN SYNDROME:-
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