Oral Pathology Marathon Flashcards
4 types of pathologies:
Developmental
Hereditary/Genetic
Familial
Congenital
Of the Genetic abnormalities, what % is unknown etiology?
% inherited ?
% known environmental causes?
85%
10%
5%
3 Characteristics of Developmental conditions:
Present at young age/congenital
Bilaterally symmetrical
Asymptomatic
Without jaw development (type of aplasia):
Small, underdeveloped jaw:
Large jaw:
Agnathia
Micrognathia
Macrognathia
Primary Macrognathia:
Secondary (acquired) Macrognathia:
Developmental
tumors, acromegaly, Paget’s
A _______ is characterized by multiple different abnormalities
Syndrome
Teeth come from what germ layer?
Ectoderm
Micrognathia is a type of _____plasia
Hypo
Cleft lip/palate is a _______ anomaly occurring ______
developmental
1st trimester
Cleft lip occurs in 1/____ white births
1/1000
T/F
The etiology of cleft palate is unknown
True
Mutations in cleft lip/palate have been shown in how many genes involved in the development of the palat/lip?
6-12 genes
The lateral palatal shelves fuse anteriorly at the junction with the _______ and fuse posteriorly
Premaxilla
The upper lip (development) is a ______ epithelium
What penetrates/develops into CT and muscle in the upper lip adding bulk?
bilayered
Mesoderm
Where does the mesoderm (forms CT/muscle in upper lip) originate?
Globular portion of median nasal process and Maxillary processes bilaterally
When a cleft forms there is a lack of ______ penetration
Mesoderm
Cleft lip is on the upper lip, off the midline, ___% bilateral
20%
Cleft palate is _____ to the Premaxilla over the _____
Anterior
Alveolar Ridge
T/F
Bifid Uvula is related to Cleft Palate
False
Bifid Uvula is associated with what?
submucosal cleft of muscle
Most common cleft?
2nd most common?
Least common?
Cleft lip with cleft palate
cleft lip
cleft palate
There are over _____ syndromes that include clefting, making up about ____% of all clefting cases.
400
30%
What is the Rule of 10’s in treating cleft lip?
When do you treat cleft Palate?
10 weeks old / 10 lbs / 10 gm% Hb
1.5 years
An oft-missed congenital malformation that may be present with other anomalies:
Lip pits