Home | About JCVJS | Editorial board | Ahead of print | Current Issue | Archives | Instructions | Subscribe | Advertise | Contact us |   Login 
Journal of Craniovertebral Junction and Spine
Search Articles   
    
Advanced search   
 


 
   Table of Contents  
CASE REPORT
Year : 2017  |  Volume : 8  |  Issue : 3  |  Page : 283-284  

Aarskog-Scott syndrome: An unusual cause of scoliosis


1 Department of Orthopedics and Traumatology, Acibadem University Atakent Hospital, Istanbul, Turkey
2 Department of Orthopedics and Traumatology, Etfal Training and Research Hospital, Istanbul, Turkey

Date of Web Publication20-Sep-2017

Correspondence Address:
Kerim Sariyilmaz
Department of Orthopedics and Traumatology, Acibadem University Atakent Hospital, Halkali Merkez Mahallesi, Turgut Ozal Bulvari, No.: 16, 34303, Kucukcekmece, Istanbul
Turkey
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jcvjs.JCVJS_133_16

Rights and Permissions
   Abstract 

A 16-year-old boy who had been diagnosed previously as Aarskog-Scott syndrome (AAS), referred to our clinic with shoulder asymmetry for 1 year. Results of spine examination showed a 52° right thoracic curve at T3-T11. Surgery was planned, and T1–L1 posterior instrumentation and fusion were performed. After surgery, satisfactory correction was achieved, and during 10 years follow-up, the patient had no complaints. AAS is a X-linked genetic disorder with facial, genital, and skeletal manifestations. Scoliosis is not reported as a typical finding of AAS, and there is no reported case in the English literature. Due to mutation affecting the developing skeleton tissue, spinal deformities may develop. In our case, concave side fusion was seen at the deformity. Although we do not know any specific pattern of the scoliotic deformity of this syndrome, surgical correction of the deformity can be difficult because of the premature fusion at these levels.

Keywords: Aarskog-scott syndrome, scoliosis, spinal deformity


How to cite this article:
Sariyilmaz K, Ozkunt O, Korkmaz M, Dikici F, Domanic U. Aarskog-Scott syndrome: An unusual cause of scoliosis. J Craniovert Jun Spine 2017;8:283-4

How to cite this URL:
Sariyilmaz K, Ozkunt O, Korkmaz M, Dikici F, Domanic U. Aarskog-Scott syndrome: An unusual cause of scoliosis. J Craniovert Jun Spine [serial online] 2017 [cited 2018 May 25];8:283-4. Available from: http://www.jcvjs.com/text.asp?2017/8/3/283/215205


   Introduction Top


Aarskog-Scott syndrome (AAS) (facio-digital-genital) was first described in 1970 by Aarskog[1] in seven males from one family with ocular hypertelorism, anteverted nostrils, a broad upper lip, and a shawl scrotum. A year later, Scott[2] emphasized the occurrence of ligamentous laxity, genu recurvatum, and flat feet. It is a rare X-linked recessive disorder and related with a mutation on FDG1 found within region Xp11.21. Typical findings include short stature, distinct craniofacial abnormalities, brachydactyly with interdigital webbing, joint laxity, and shawl scrotum. A variety of other skeletal malformations is observed including cervical spine abnormalities such as odontoid hypoplasia, congenital vertebral anomalies, spina bifida occulta, and additional pairs of the rib. To the best of our knowledge, there has been no case about AAS with scoliosis in English literature. In this case report, we present an adolescent scoliosis patient who was previously diagnosed as AAS and treated by posterior instrumentation and fusion.


   Case Report Top


A 16-year-old boy is referred to our clinic with shoulder asymmetry for 1 year. He had been diagnosed as AAS previously. He had short stature (145 cm), macrocephaly, broad upper lip with long philtrum, ocular hypertelorism, shawl scrotum, and brachydactyly. He had no mental retardation. Results of spine examination showed a right thoracic scoliosis with an elevation of the ipsilateral shoulder [Figure 1]a. Neurological examination was completely normal.
Figure 1: (a) Clinical photo of the spine and typical face findings of Aarskog-Scott syndrome (b) Preoperative X-ray

Click here to view


Standing anteroposterior spinal radiographs obtained and a 52° right thoracic curve at T3-T11 was observed [Figure 1]b. Concave side fusion was seen between T5 and T9 levels. Surgery was planned for this deformity. Preoperative lateral bending radiograph showed correction of the curve to 28°, and traction radiograph showed an angle of 24°. Posterior thoracic approach with transpedicular instrumentation, correction, and fusion was performed between T1 and L1 vertebrae. During surgery, fusion at the apical concave side was observed. After placement of the pedicle screws, correction was achieved by rod derotation maneuver. Satisfactory correction of the sagital and coronal plane was obtained, and coronal Cobb angle was measured 16° after surgical correction and thoracal hump disappeared. Patient mobilized on 2nd day postoperatively, and shoulder asymmetry resolved [Figure 2]a. At 10 years follow-up, no shoulder and pelvic asymmetry were observed. Radiographs showed a slight increase of the Cobb angle, which was 18°. No adding-on was observed below the instrumentation level; however, slight right trunkal tilt and 3.3 cm coronal imbalance were observed [Figure 2]b.
Figure 2: (a) Early postoperative X-ray (b) 10 years follow-up X-ray

Click here to view



   Discussion Top


AAS is an X-linked genetic disorder with facial, genital, and skeletal manifestations. An autosomal recessive and autosomal dominant inheritance have also been reported. FDG1 mutation is responsible for this syndrome, and this mutation appears to affect the developing skeleton tissue during the onset of ossification in regions of endochondral and intramebranous ossification including craniofacial bones, vertebrae, ribs, long bones, and phalanges, thus skeletal abnormalities dominate the clinical manifestations of the syndrome.[3] Gorski et al.[3] reviewed the spectrum of skeletal abnormalities reported in the literature more than 110 patients. Skeletal abnormalities of this syndrome include short stature, delayed oossification centers, hypertelorism, maxillary hypoplasia, broad nasal bridge, cervical spine anomalies, rib and sternal anomalies, short/broad hands, brachydactyly, hypoplastic phalanges, syndactyly, and joint laxity. No scoliosis patient was reported in this review. In the literature, there is no English report about AAS and scoliosis. To the best of our knowledge, only one case reported an AAS patient with scoliosis, in German, by Fehlow et al.[4] They reported a 22-year-old patient with AAS who had a scoliosis causing a radicular impairment with resulting severe paresis of the right fibular nerve. The patient was also associated with mental retardation, epilepsy, premature craniosynostosis, and tardive dyskinesias. However, this mental retardation is atypical for AAS because Logie and Porteous,[5] reported normal IQ levels in 21 AAS patients. Our patient had a single thoracic curve recognized 1 year before admission. We do not know the nature of the curve whether it is progressive or not. We could not follow the patient because the curve was already 53°, thus surgery was addressed. Only thoracic fusion was performed similar to idiopathic-like curves and during 10 years follow-up, no decompensation was developed. The distinct feature of the curve was the concave side fusion. Although we do not know any specific pattern of the scoliotic deformity of this syndrome, surgical correction of the deformity can be difficult because of the premature fusion at these levels.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Aarskog D. A familial syndrome of short stature associated with facial dysplasia and genital anomalies. J Pediatr 1970;77:856-61.  Back to cited text no. 1
[PUBMED]    
2.
Scott CI. Unusual facies, joint hypermobility, genital anomaly and short stature: A new dysmorphic syndrome. Birth Defects Orig Artic Ser 1971;7:240-6.  Back to cited text no. 2
    
3.
Gorski JL, Estrada L, Hu C, Liu Z. Skeletal-specific expression of Fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome). Dev Dyn 2000;218:573-86.  Back to cited text no. 3
    
4.
Fehlow P, Miosge W, Walther F. Aarskog syndrome in association with mental and psychological retardation, grand mal epilepsy and tardive dyskinesia and apparent radicular paralysis of the fibular nerve in torsion scoliosis. Padiatr Grenzgeb 1993;31:345-51.  Back to cited text no. 4
    
5.
Logie LJ, Porteous ME. Intelligence and development in Aarskog syndrome. Arch Dis Child 1998;79:359-60.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2]



 

Top
  
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
   Case Report
   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed357    
    Printed1    
    Emailed0    
    PDF Downloaded0    
    Comments [Add]    

Recommend this journal