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ABSTRACT
The aim of this study was to investigate the prevalence of hypodontia among patients who were
treated in three main hospitals namely Prince Ali Hospital, Zaid Hospital and Princess Haya Hospital
located in southern Jordan.
A total of 1726 orthodontic patients were included in the study with an age range between 12 and
25 years. Patients with cleft lip and palate, ectodermal dysplasia, or having tooth loss due to caries,
trauma, periodontal disease or congenitally missing third molars were excluded from the study. Dental
history and panoramic radiographs were used in the diagnosis of congenitally missing teeth.
The prevalence of hypodontia was 7.1% excluding third molars; 2.10% were males and 5.01% were
females. The total number of missing teeth was 197. The most commonly missing teeth were maxillary
lateral incisors, followed by maxillary and mandibular second premolars. The number of missing teeth
were greater in the maxilla than in the mandible. Hypodontia was almost equally distributed between
both sides of jaws. There was significant difference between the type of malocclusion and the number
of missing teeth. The majority of patients had one or two missing teeth.
Key words: Hypodontia, congenitally missing teeth, prevalence, Jordan
INTRODUCTION
Hypodontia is one of the most common dental
developmental anomaly in human being. In literature
many terms have been used to describe the reduction
in number of teeth: hypodontia, oligodontia, congenitally missing teeth; namely, aplasia of teeth, anodontia, and agenesis of teeth.
The term hypodontia was most frequently used.
Some authors prefer to use the term agenesis of teeth
as it describes more accurately the developmental
disorder involved.1
The cause of tooth agenesis may be due to environmental factors such as radiation, chemotherapy2 or
hereditary. Congenitally missing teeth may be transmitted as autosomal dominant, autosomal recessive or
X linked genetic condition.3-6 Its occurrence may be
isolated or non-syndromatic hypodontia and hypodontia
associated with syndromes.7 Tow mutated genes in
human, MSX1 and PAX are known to cause agenesis of
permanent teeth.8, 9
The absence of one or two teeth is relatively
com-mon, but sever hypodontia is rare and may be
1
2
Correspondence: Fuad Hamed Almoherat, Wadi Elseer PO Box 53, Amman, Jordan, Email:
fuadalmoherat@yahoo.com
Pakistan Oral & Dental Journal Vol 29, No. 1, (June 2009)
45
Patients with
Hypodontia n (%)
Total n (%)
Male
Female
Total
36 (2.1%)
87 (5.0%)
123 (7.1%)
589 (34.1%)
1041 (58.8%)
1603 (92.9%)
625 (36.2%)
1101 (63.8%)
1726 (100%)
Male n (%)
Female n (%)
Total n (%)
12 ( 6.1% )
16 ( 8.1% )
4 ( 2.0% )
7 (3.6%)
6 (3.0%)
8 (4.1%)
4 (2.0%)
5 (2.5%)
0
0
0
0
62 (31.5%)
33 (16.8%)
26 (13.2%)
6 (3.0%)
22 (11.2%)
9 (4.6%)
18 (9.1%)
7 (3.6%)
9 (4.6%)
1 (1.0%)
2 (1.0%)
1 (1.0%)
1 (1.0%)
135 (68.5%)
45 (22.8%)
42 (21.3%)
10 (5.1%)
29 (14.7%)
15 (7.6%)
26 (13.2%)
11 (5.6%)
14 (7.1%)
1 (1.0%)
2 (1.0%)
1 (1.0%)
1 (1.0%)
197 (100%)
Pakistan Oral & Dental Journal Vol 29, No. 1, (June 2009)
46
Total n (%)
Male
Female
Total
19 (15.4%)
53 (43.1%)
72 (58.5%)
12 (9.8%)
27 (22%)
39 (31.7%)
5 (4.1%)
7 (5.7%)
12 (9.8%)
36 (29.3%)
87 (70.1%)
123 (100%)
Total n (%)
39 (31.7%)
26(21.1%)
7 (5.7%)
72 (58.5%)
24 (19.5%)
9 (7.3%)
6 (4.9%)
39 (31.7%)
2 (1.6 %)
0 (0%)
10 (8.1%)
12 (9.8%)
65 (52.8%)
35 (28.5%)
23 (18.7%)
123 (100%)
2
3
4.
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13
14
15
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