Literature DB >> 3877092

A morphometric analysis of the craniofacial configuration in achondroplasia.

M M Cohen, G F Walker, C Phillips.   

Abstract

Human achondroplasia can be viewed as an experimental model for studying the effects of abnormal endochondral bone formation on the development of the skull as a whole. In this study, lateral cephalograms of 25 adult males and 26 adult females with achondroplasia were converted to a two-dimensional coordinate model of craniofacial morphology and analyzed using 66 linear, angular, and area variables. Lateral cephalograms of 951 normal adults were used for comparison. Two sample t-tests were used to compare achondroplastic cephalograms with normal cephalograms. Multivariate statistical analysis included Hotelling's T2 and discriminant function analysis. Selected variables were graphed as profile patterns in which mean values were expressed as standard deviation units (Z scores) relative to the norm. Finally, Calcomp plots were used for visual inspection and for comparison of the average cephalometric tracings of male and female achondroplastic subjects with normal male and female subjects, respectively. Significant findings in achondroplasia included enlarged calvaria, frontal bossing, large frontal sinuses, occipital prominence, normal anterior cranial base length, strikingly shortened posterior cranial base length, an acute cranial base angle, a short nasal bone that was deformed and depressed, short upper facial height, recessed maxilla, posterior tilt of the nasal floor, and a prognathic mandible that was anteriorly displaced but of normal size with a normal gonial angle and a high coronoid process. The finding of normal anterior cranial base length in achondroplastic subjects was surprising since the cranial base is preformed in cartilage and hypoplasia and shortening would be expected. Since the brain is enlarged in achondroplasia, the expanding frontal lobes may possibly influence the growth of the anterior cranial base, since it is known to follow a neural pattern of growth. Cribriform plate length was strikingly reduced, but anterior sphenoidal length was strikingly increased, compensating for the shortened cribriform plate length and suggesting that growth in the length of the anterior cranial base takes place primarily by adaptation at one site--namely, the sphenoethmoidal synchondrosis. Strikingly short posterior cranial base length was interpreted as resulting from hypoplasia of bone that is preformed in cartilage with possible early closure of the spheno-occipital synchondrosis. The exaggerated closure of the cranial base angle in achondroplasia may be related to an increased brain size and possibly earlier than normal closure of the intersphenoidal synchondrosis.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1985        PMID: 3877092

Source DB:  PubMed          Journal:  J Craniofac Genet Dev Biol Suppl        ISSN: 0890-6661


  9 in total

Review 1.  FGFR3-related dwarfism and cell signaling.

Authors:  Daisuke Harada; Yoshitaka Yamanaka; Koso Ueda; Hiroyuki Tanaka; Yoshiki Seino
Journal:  J Bone Miner Metab       Date:  2008-12-09       Impact factor: 2.626

2.  Morphological integration between the cranial base and the face in children and adults.

Authors:  Nikolaos Gkantidis; Demetrios J Halazonetis
Journal:  J Anat       Date:  2011-02-16       Impact factor: 2.610

Review 3.  Achondroplasia: a comprehensive clinical review.

Authors:  Richard M Pauli
Journal:  Orphanet J Rare Dis       Date:  2019-01-03       Impact factor: 4.123

4.  Breathing abnormalities in sleep in achondroplasia.

Authors:  K A Waters; F Everett; D Sillence; E Fagan; C E Sullivan
Journal:  Arch Dis Child       Date:  1993-08       Impact factor: 3.791

5.  Bilateral ossiculoplasty in 1 case of achondroplasia.

Authors:  Jongyoon Jung; Chulwon Yang; Sunkyu Lee; June Choi
Journal:  Korean J Audiol       Date:  2013-12-13

Review 6.  Craniofacial morphology and dental maturity in children with reduced somatic growth of different aetiology and the effect of growth hormone treatment.

Authors:  Sotiria Davidopoulou; Athina Chatzigianni
Journal:  Prog Orthod       Date:  2017-04-27       Impact factor: 2.750

Review 7.  FGF23 and its role in X-linked hypophosphatemia-related morbidity.

Authors:  Signe Sparre Beck-Nielsen; Zulf Mughal; Dieter Haffner; Ola Nilsson; Elena Levtchenko; Gema Ariceta; Carmen de Lucas Collantes; Dirk Schnabel; Ravi Jandhyala; Outi Mäkitie
Journal:  Orphanet J Rare Dis       Date:  2019-02-26       Impact factor: 4.123

Review 8.  Cranial Base Synchondrosis: Chondrocytes at the Hub.

Authors:  Shawn A Hallett; Wanida Ono; Renny T Franceschi; Noriaki Ono
Journal:  Int J Mol Sci       Date:  2022-07-15       Impact factor: 6.208

9.  Meckel's and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible.

Authors:  Martin Biosse Duplan; Davide Komla-Ebri; Yann Heuzé; Valentin Estibals; Emilie Gaudas; Nabil Kaci; Catherine Benoist-Lasselin; Michel Zerah; Ina Kramer; Michaela Kneissel; Diana Grauss Porta; Federico Di Rocco; Laurence Legeai-Mallet
Journal:  Hum Mol Genet       Date:  2016-06-03       Impact factor: 6.150

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.