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. 2011 Jul;81(4):578-83.
doi: 10.2319/102210-618.1. Epub 2011 Feb 21.

Cephalometric features in isolated growth hormone deficiency

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Cephalometric features in isolated growth hormone deficiency

Luiz Alves Oliveira-Neto et al. Angle Orthod. 2011 Jul.

Abstract

Objective: To analyze cephalometric features in adults with isolated growth hormone (GH) deficiency (IGHD).

Materials and methods: Nine adult IGHD individuals (7 males and 2 females; mean age, 37.8 ± 13.8 years) underwent a cross-sectional cephalometric study, including 9 linear and 5 angular measurements. Posterior facial height/anterior facial height and lower-anterior facial height/anterior facial height ratios were calculated. To pool cephalometric measurements in both genders, results were normalized by standard deviation scores (SDS), using the population means from an atlas of the normal Brazilian population.

Results: All linear measurements were reduced in IGHD subjects. Total maxillary length was the most reduced parameter (-6.5 ± 1.7), followed by a cluster of six measurements: posterior cranial base length (-4.9 ± 1.1), total mandibular length (-4.4 ± 0.7), total posterior facial height (-4.4 ± 1.1), total anterior facial height (-4.3 ± 0.9), mandibular corpus length (-4.2 ± 0.8), and anterior cranial base length (-4.1 ± 1.7). Less affected measurements were lower-anterior facial height (-2.7 ± 0.7) and mandibular ramus height (-2.5 ± 1.5). SDS angular measurements were in the normal range, except for increased gonial angle (+2.5 ± 1.1). Posterior facial height/anterior facial height and lower-anterior facial height/anterior facial height ratios were not different from those of the reference group.

Conclusions: Congenital, untreated IGHD causes reduction of all linear measurements of craniofacial growth, particularly total maxillary length. Angular measurements and facial height ratios are less affected, suggesting that lGHD causes proportional blunting of craniofacial growth.

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Figures

Figure 1
Figure 1
Profile of a female patient (age 55) with isolated and untreated growth hormone deficiency.
Figure 2
Figure 2
Cephalometric landmarks: A, point A; ANS, anterior nasal spine; Ar, articular; B, point B; Gn, gnathion; Go, gonion; Me, menton; N, nasion; S, sella turcica; Or, orbital; Po, porion; Co, condylion.
Figure 3
Figure 3
Standard deviation scores (SDS) for cephalometric features of untreated isolated growth hormone deficiency (IGHD). Values lower than −2 or higher than +2 are by definition abnormal. (a) P < .001 in comparison with the other linear measurements. (b) P < .001 for both lower-anterior facial height and mandibular ramus height in comparison with other linear measurements. (c) P < .001 in comparison with the other angular measurements (analysis of variance [ANOVA] with the Tukey test).

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