lecture 8 effect of systemic ds on periodontal ds Flashcards
what type of periodontitis for major impact
severe/early-onset periodontitis
what type of periodontitis for moderate impact?
- chronic periodontitis
- increase prevalance
systemic disorders cause –>
loss of periodontal tissue
what three things can influence periodontal inflammation
- genetic disorder
- acquired immunodeficiency ds
- inflammatory ds
what ds is associated with this oral presentation
- oral presentation of Down Syndrome
- moderate to severe periodontitis with rapid progression
- local factors do not explain the severity of the periodontal destruction
- intrinsic immune system defects
explain what leukocyte adheesion deficiency is
- a mutation in beta-2 integrin gene where there is a lack of them in leukocytes.
- This causes for low integrin expression on the neutrophils so
- neutrophils are confined to blood vessels (loose neutrophil-associated homeostasis)
oral manifestations seen in LAD
- severe gingial inflammation, acute gingival lesions
- early-onset and rapidly progressive alveolar bone loss
- early loss of the primary AND perm teeth
*not just oral but history of recurrent inection but with no pus
what ds is this oral presentation associated with?
LAD leukocyte adhesion deficiency
- severe gingial inflammation, acute gingival lesions
- early-onset and rapidly progressive alveolar bone loss
- early loss of the primary AND perm teeth
describe papillon-lefevre syndrome
mutations in the cathepsin C gene which can compromise neutrophil function
can have hyperkeratotic lesions
if we have a pt with hyperkeratotic lesions on palms, soles of feet, elbow and/or knees with periodontal inflammation what could it be
papillon-lefevre syndroms
oral presentation of papillon-lefevre
- severe gingival inflammation
- early-onset and rapidly progressive alveolar bone loss
- early loss of the primary and permanent teeth
describe chediak-higashi syndrome
- a mutation in gene (CHS1 and LYST) which can cause albinism, pyogenic infections, and varying neurologic problems
some clinical S&S of Chediak-Higashi Syndrome
- partial oculocutaneous albinism which can cause defects in melanin granules
- recurrent pyogenic infections
- varying neurologic probs like intellectual deficit and dementia
oral manifestations seen in Chediak-higashi Syndrome
- severe gingival inflammation
- Early-onset and rapidly progressive alveolar bone loss
- Early loss of the primary and perm teeth
- Poor response to dental tx
describe congenital neutropenia
Mutations in ELANE (50%), HAX1 (10%) gene.
A decrease # and dysfunction of neutrophils, and defficient in immune response so lots of severe and recurrent infections
what are the ds associatd with immunologic disoders
- Down syndrome
- LAD
- Papillon Lefevre
- Chediak-higashi syndrome
- Congenital neutropenia
what are the ds affecting the oral mucosa and gingival tissue
- epidermolysis bullosa
describe epidermolysis bullosa
aka Kindler Syndrome
a mutation in the fermitin family homologue 1 gene.
Has a lack of integrin activiation which affects the keratinocyte cell adhesion which can lead to defects in basement membrane zones as well.
Recurrent blister formation
Photosensitivity
oral manifestations of epidermolysis bullosa
oral blisters, severe periodontitis, and you need immunofluorescence to confirm dx
what are the ds affecting the CT
- ehlers danlos syndrome
describe ehlers-danlos syndrome
a mutation in genes encoding fibrillar collagens or enzymes in the biosynth
it affects collegen production and composition so pts will have joint hypermobility, skin extensibility and tissue fragility