Shape of the craniofacial complex in patients with Klinefelter syndrome.

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The shape and size of the craniofacial complex in 35 adults with Klinefelter syndrome (47,XXY) were analyzed cephalometrically and compared with 60 control males. Twenty-four angular and 18 linear measurements were obtained for each subject. The results showed that the 47,XXY males were different from the controls in several areas of the craniofacial skeleton. Most of the differences were located in the cranial base and the cranial base angle (p < 0.02). The length of the maxillary base was greater (p < 0.05) and more prognathic (p < 0.01) in the study group. The mandible was also longer and more prognathic (p < 0.01).

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summary Occlusal plane position was analysed cephalometrically in 35 Klinefelter adults (47, XXY) and compared with 60 eugnath control males (46, XY).The significantly smaller angles between the occlusal plane and the cranial base (NSL‐OLs) and between the occlusal plane and the Frankfort horizontal plane (Fr‐OLs) were obtained in 47, XXY males (P &lt; 0.0l), while the angles between the maxillary base and the occlusal plane (NL‐OLs) and between the Camper's line and the occlusal plane (Camp.‐OLs) were not significantly different (P &gt; 0.05) from the control group. Significantly smallelr angles between the occlusal plane and the cranial base (NSL‐OLs) and between the occlusal plane and the Frankfort horizontal plane (Fr‐OLs) in Klinefelter males are attributed to the hereditary influence of an extra X chromosome on the smaller growth of the cranial base and the greater growth of the lower border of the mandible. Although the maxilla was also shifted forward in XXY males in relation to the cranial base it was not enough to compensate for the hereditary influence, due to the greater growth of the lower border of the mandible and the smaller cranial base in 47, XXY males, on the inclination of the occlusal plane to the Frankfort horizontal plane and the cranial base. The forward shift of maxilla was sufficient to compensate for the inclination of the occlusal plane in 47, XXY males to the maxillary base and the Camper's line (P &gt; 0.05).

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Occlusal plane orientation in Klinefelter syndrome (47,XXY males).
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Occlusal plane position was analysed cephalometrically in 35 Klinefelter adults (47,XXY) and compared with 60 eugnath control males (46,XY). The significantly smaller angles between the occlusal plane and the cranial base (NSL-OLs) and between the occlusal plane and the Frankfort horizontal plane (Fr-OLs) were obtained in 47,XXY males (P < 0.01), while the angles between the maxillary base and the occlusal plane (NL-OLs) and between the Camper's line and the occlusal plane (Camp.-OLs) were not significantly different (P > 0.05) from the control group. Significantly smaller angles between the occlusal plane and the cranial base (NSL-OLs) and between the occlusal plane and the Frankfort horizontal plane (Fr-OLs) in Klinefelter males are attributed to the hereditary influence of an extra X chromosome on the smaller growth of the cranial base and the greater growth of the lower border of the mandible. Although the maxilla was also shifted forward in XXY males in relation to the cranial base it was not enough to compensate for the hereditary influence, due to the greater growth of the lower border of the mandible and the smaller cranial base in 47, XXY males, on the inclination of the occlusal plane to the Frankfort horizontal plane and the cranial base. The forward shift of the maxilla was sufficient to compensate for the inclination of the occlusal plane in 47, XXY males to the maxillary base and the Camper's line (P > 0.05).

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Surgical orthodontic correction of acromegaly with mandibular prognathism.
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  • Takakaza Yagi + 2 more

A male (30 years five months) who complained of mandibular prominence and masticatory dysfunction was diagnosed as a mandibular prognathic with acromegaly after cephalometric and endocrine examinations. The level of growth hormone (GH) subsequent to a transsphenoidal hypophysectomy had been controlled by medicines for about five years. Surgical orthodontic correction improved his occlusion and profile, but magnetic resonance imaging detected a recurrent adenoma in the cranial base during the retention period. The recurrence resulted in slight prognathic changes of the patient with a high level of GH. This is a case report of the treatment of an acromegalic patient discussing growth considerations that could influence the orthodontic treatment plan and long-term stability.

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