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Physical Medicine and Rehabilitation Unit, University of Pavia, Rehabilitation Unit, IRCCS Policlinico San
3
4
University of Pavia Rehabilitation Unit, Don Carlo Gnocchi Foundation Salice Terme, Italy
Corresponding author:
GABRIELLA CARENZIO
E-‐mail:g.carenzio@smatteo.pv.it
Background. Congenital Muscular Torticollis (CMT) is the most common form of torticollis
in infants;; on clinical presentation it is classified into 3 types: (i) postural torticollis, with
postural deformity only in the neck, (ii) muscular torticollis, where neck deformity is
associated with muscle tightness and restricted passive range of motion (ROM), and (iii)
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Aim. The aim of this study was to evaluate the physical therapy outcome of infants with
CMT treated either by parents using a home exercise program, or by a physical therapist.
Setting. Outpatients with CMT at our Department of Physical Medicine and Rehabilitation.
Population. Fifty consecutive newborns with CMT, referred by the primary pediatrician:
Methods. In our study, 50 infants with CMT were evaluated and treated either by a
physical therapist or by parents using a home program.
Results. 16 females (32%) and 34 males (68%), aged 10.2 weeks (SD 6.66). 23 of the
infants (46%) presented with more severe articular limitations than the others (p=0.002)
and were therefore prescribed outpatient treatment by a physical therapist;; the remaining
27 less severe cases (54%) were prescribed a home therapy program. 49 infants achieved
full resolution after an average of 81.06 days (SD 64.05) of rehabilitation treatment. The
group of patients who were treated at home achieved resolution more quickly (72.8 vs
91.1 days), although statistical significance was not reached.
Conclusions. Infants with CMT who were treated early, either at home or in the outpatient
clinic, completely recovered normal neck movement in a short time. It is important not to
discharge patients until they have achieved full resolution of CMT symptoms to exclude
the minimal risk of relapse.
Clinical Rehabilitation Impact. This study demonstrates the importance of early
treatment in cases of Congenital Muscular Torticollis.
Introduction
Congenital Muscular Torticollis (CMT) 1,2,3,4,5,6,7 is a benign pathology mainly characterised
by the thickening and shortening of the sternocleidomastoid muscle (SCM), which results
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in head tilt and limited head rotation. Torticollis may be present at birth, or may not appear
until 2-4 weeks postdelivery. 3,4 In addition to the characteristic head posture with lateral
neck flexion and rotation to the contralateral side, a mass or tightness may be felt in the
muscle belly of the affected SCM. 3,4,580% of torticollis cases in newborns are CMT 8 , with
a variable incidence of 0.084%-3.92%. 1,3,5 CMT is the third most common congenital
musculoskeletal disorder after hip dysplasia and clubfoot. 9,10,11 The condition occurs more
frequently on the left side 11 and is rarely bilateral 12,13;; it affects more males than females,
with a ratio of 3:2 4,9;; there is a positive family history in 10% of cases.14
CMT may be associated with metatarsus adductus, congenital hip dysplasia (0-29%
variation) 9,15,16, plagiocephaly 17, craniofacial asymmetry 18,19, and brachial plexus injury. 8
Since 1992 there has been an increase in cases of CMT and positional plagiocephaly
contribute to the application of the guidelines for the prevention of Sudden Infant Death
Syndrome by the American Academy of Pediatrics, who discourage the prone sleeping
position. 20,21,22
Although the etiology of CMT remains unclear, there are some well-substantiated
hypotheses, including intrauterine malposition that causes an ischemic event, fibrosis of
the SCM leading to a compartment syndrome, birth-trauma 11,26,27,28,29 hereditary
hypothesis 30, and neurogenic involvement or infection.
CMT may also be present in newborns delivered by cesarean section, and there is no
significant difference in the clinical severity of CMT based on type of delivery. 31
If CMT is developed prior to delivery, it may cause birth trauma or breech birth.
Oligohydramnios is thought to be a risk factor for the development of both torticollis and
hip dysplasia. 1
The diagnosis of CMT is clinical and involves assessment of the incorrect neck and head
movement, palpation of the SCM, and measurement of ROM in neck rotation (where 100°
is normal in infants) and lateral flexion (where 65° is normal). 6 Ultrasound imaging of the
SCM is currently considered to be the most reliable means of diagnosis. 32,33,34,35,36,37
More specialized diagnostic tests such as X-ray, MRI or CT scan can rule out the
presence of other pathologies that can cause torticollis: Klippel-Feil syndrome, posterior
fossa tumors, Sandifer syndrome, 38 spasmodic torticollis, atlas malformation, respiratory
tract infection,1 cervical adenitis. 5,8,39,40,41 Particular attention should be paid to certain ocular
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diseases where asymmetrical posturing of the head is an effective mechanism for
compensating ocular defects. 42,43
Early diagnosis is essential in order to begin rehabilitation therapy as early as possible,
thus avoiding the thickening and shortening of the SCM that causes tilt and rotation of the
head, and deformation of the face and skull.
Parents are often the first to report the appearance of torticollis to the pediatrician, usually
when infants are between 2 and 4 months old.
Previous studies agree that if rehabilitation treatment is not carried out within the first year
of life, recovery of neck ROM is reduced. 3,4,6,7,13,21,26,32,44
The physical therapy management of CMT includes passive stretching and positioning
away from the tightness for active movements.
It is very important for parents/caregivers to be taught how to correctly implement the
home therapy program. 6,7,44,45
In severe cases, the use of an orthopedic collar or botulinum toxin injections 46 in addition
to physical therapy offers a 60-90% chance of resolution.
Surgical release is only used if infants do not respond to conservative interventions after
12 months of age. 13,24,47,48
The aim of this study was to evaluate physical therapy outcomes in infants with CMT
treated either by parents using a home exercise program or by a physical therapist.
50 consecutive newborns with CMT, who had been referred by the primary pediatrician,
were assessed by a Physical and Rehabilitation Medicine (PRM) physician between
March 2006 and September 2013.
Data were collected over a 7-year period but no significant changes were detected in
nursery care or birth practices.
During clinical evaluation, the following health history factors were collected: sex, type of
delivery, weight at birth and age at initial visit.
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Rehabilitation program
On the basis of the severity of ROM limitations and parent compliance observed during
clinical evaluation, an individual r ehabilitation program was designed b
y PRM physician to
be implemented either by a physical therapist in the outpatient clinic, or by the
parents/caregivers at home. The parents/caregivers of infants who were prescribed home
therapy programs were taught how to perform the exercises, and were strongly
recommended to treat infants whenever possible using exercises and caregiving
maneuvers.
When parents seemed unsure of whether or how to carry out the necessary exercises, the
physician asked them to lie in a prone position and demonstrated the correct passive
rotation and lateral flexion movements on the parents themselves.
Outpatients were treated by a physical therapist for 30 minutes each day, until discharge.
Passive cervical rotation and lateral flexion could be peformed when infants were asleep
or awake depending on compliance, which is usually greater in newborns between 0 and 2
months old.
Active movements were encouraged during playtime by showing infants toys or attracting
their attention with sounds or lights.
Infants were assessed once a month during therapy and then one month after complete
resolution in order to verify outcome stability. Parents were actively encouraged to
continue performing the rehabilitation exercises for a few months to maintain recovery.
Statistical Analysis
Descriptive statistics were produced for demographic characteristics for this study sample
of patients. The Shapiro-Wilk test was used to test the normal distribution of quantitative
variables;; all variables were normally distributed and so the results were expressed as
mean values and SD (standard deviation);; qualitative variables were summarized as
counts and percentages. For quantitative variables, a t-test was used for independent data
to analyse differences between two groups, and chi-square or Fisher exact test, as
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appropriate, was used for qualitative variables. All tests were two sides and p<0.05 was
considered statistically significant.
Data analysis was performed using the STATA statistical package (release 13.1, 2014,
Stata Corporation, College Station, Texas, USA).
Results
50 consecutive newborns with CMT were assessed in the outpatient clinic at the
Department of Physical Medicine and Rehabilitation: 16 female (32%) and 34 male (68%),
mean age 10.2 weeks (SD 6.66) at initial visit.
30 subjects (60%) were delivered vaginally (9 female and 21 male), 14 (28%) were
delivered with cesarean section (5 female and 9 male), 2 (4%) were delivered preterm (1
female and 1 male), and 4 (8%) were delivered with instruments following dystocia (1
female and 3 male).
The mean birth weight was 3239 grams (SD 529.6), without significant difference
(p=0.137) between female and male subjects (3076 grams, SD 677, and 3315 grams, SD
435, respectively).
The right side was affected in 26 subjects (52%), and the left side in 24 (48%).
Clinical evaluation
All the subjects had torticollis but met age-appropriate developmental milestones. None of
the subjects had hip dysplasia.
Plagiocephaly was present in 8 subjects (16%), 6 female and 2 male.
SCM palpation
19 subjects ( 38%) had no mass or tightness in the SCM.
13 subjects (26%) had mass and tightness in the SCM.
18 subjects (36%) had tightness but no mass in the SCM.
CERVICAL ROM
The results of the goniometric measurement of the rotation and lateral flexion of the
cervical spine, divided into 4 distinct ranges, were as follows:
- 25 subjects (50%) had complete passive ROM in rotation and lateral flexion, but
limitations in active ROM (postural torticollis),
- 15 subjects (30%) had mild limitation in lateral flexion (5 subjects) or rotation (3
subjects) or both (7 subjects),
- 6 subjects (12%) had moderate limitation in lateral flexion (2 subjects) or rotation (3
subjects) or both (1 subject),
- 4 subjects (8 %) had severe limitation in both rotation and lateral flexion.
Ultrasound imaging was performed for 28 subjects (52%) only in the presence of severe
limitation, muscle mass or severe tightness. It was not performed for newborns with
complete or mild limitation, or absence of muscle mass or tightness.
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- 10 subjects (20%) showed no signs of mass or tightness in the SCM,
- 11 subjects (22%) had a fibrous SCM mass or increased thickness of the SCM,
- 7 subjects (14%) had muscle hematoma.
Rehabilitation treatment
Home e xercise program: in 27 cases (54%) a PRM physician taught parents/caregivers
how to perform the torticollis rehabilitation program at home, and planned monthly
follow-up visits that continued until one month after resolution.
Outpatient treatment: 23 subjects (46%) were treated by a physical therapist in the
outpatient clinic. 14 subjects (28%) only needed one cycle of physical therapy ( 1 cycle =
10 sessions of 30 minutes daily ), 4 subjects (8%) needed 2 cycles, 4 subjects needed 3
cycles and only 1 subject needed 6 cycles.
Considering the severity of ROM limitation i n rotation and lateral flexion (mild limitation
<15°, moderate limitation 15-30°, severe limitation >30°), the most serious cases of
torticollis (moderate plus severe) were treated in the outpatient clinic: 9/23 (39.1%) vs
home treatment: 1/27 (3.7%);; p < 0.001.
Outcome
All but one of the newborns included in our study achieved complete recovery of neck
posture and cervical motility in an average of 81.06 (SD 64.05) days. The data
demonstrate that lateral flexion was recovered more quickly (mean days 113, SD 90.3)
than rotation (mean days 128, SD 102.2), although statistical significance was not
reached.
Resolution was not correlated with sex, age at initial visit or type of treatment;; however,
the infants treated at home with less severe passive and active ROM limitations achieved
resolution more quickly than the infants treated in the outpatient clinic by a physical
therapist (72.8 days, SD 50.7 vs 91.1 days, SD 77.4).
The only infant who did not achieve complete resolution before the age of 12 months was
referred to the orthopedic surgeon. At the first evaluation he had severe limitation of
cervical ROM in rotation and inclination. He was given 60 sessions of physical therapy
with a therapist. He is most likely not to have recovered due to his severe f ibrosis of the
SCM, as shown by ultrasound imaging.
In 3 cases (2 infants with a hematoma and 1 with a fibrous mass in the SCM) there was a
relapse of torticollis after the follow up visit one month after full resolution, so the infants
needed further treatment in the outpatient clinic and a subsequent observation period until
resolution was stable. All 3 of these infants were 6 weeks old at their initial visit and
received a total of 3 cycles of physical therapy. They achieved resolution of CMT
symptoms in an average of 67.7 days (min 43, max 98).
Discussion
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All but one of the infants in our study achieved full resolution of CMT symptoms. All the
infants were diagnosed early and treated, either in the outpatient clinic or at home, at
about 2.5 months. This age corresponds with the typical onset of torticollis reported in the
literature: 2-4 months. 39,50
Our study found that the duration of treatment before resolution was about 2.5 months
(mean 81 days, SD 64), whereas Petronic 44 had previously reported that when
rehabilitation began before 1 month of age, 98% achieved near normal ROM within 1.5
months, but when rehabilitation began after 1 month of age, treatment lasted about 6
months with fewer infants achieving near normal ROM.
Furthermore, there was a lower incidence of associated postural plagiocephaly in our
study than in others: 16% (8 cases) in our study group vs 20%-48% in previous
studies. 16,18
Our study also differs from the literature in terms of the side affected in CMT: we didn’t find
a statistically significant difference (52% right, 48% left), while the most commonly affected
side has been reported to be the left. 4
Based on the clinical evaluation, 27 (54%) of the infants in our study were prescribed a
home therapy program and parents/caregivers were taught how to conduct the exercises
by a physical therapist. It was sometimes necessary to demonstrate the passive lateral
flexion and rotation movements on the parents themselves to improve confidence and
convince them that they would not harm their child.
The remaining 23 (46%) infants were found to have more severe articular limitation than
those treated at home, with a statistically significant difference (respectively p: 0.0008, p:
0.002), so they were treated by a physical therapist in the outpatient clinic and parents
were encouraged to repeat the exercises at home.
Some authors suggest that treatment by a physical therapist may be more efficient in
achieving a normal range of motion and symmetrical movements than when
parents/caregivers are the sole providers of home exercises programs. 49
The infants in our study who were treated at home achieved resolution more quickly than
the infants treated in the outpatient clinic, respectively an average of 72.8 days compared
to 91.1, although statistical significance was not reached. This difference demonstrates
that we prescribed the correct type of treatment based on the severity of ROM limitations
in cervical rotation and lateral flexion.
Our study group achieved full resolution in a shorter time than has previously been
reported 44 , a difference that can probably be explained by the less severe articular
limitation present in our subjects: 25 infants (50%) had complete ROM at the initial visit
(postural torticollis), and only 4 infants (8%) had severe ROM limitation (>30°).
The earlier infants are treated, the better their outcome because their muscles have higher
elasticity and they are more pliable in the first 2 months of life. 6,7,50 This pliability leads to
higher infant cooperation, and, in turn, to better parent adherence to home programs.his
Our results show that ROM limitations in lateral flexion are resolved in a shorter time
(mean 113 days) than limitations in rotation (mean 128 days).
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On the basis of our observation, infants seem to tolerate passive lateral flexion exercises
better than passive rotation exercises. We also noticed that active rotation is easily
encouraged by attracting infants’ attention with sounds or lights.
The three cases (6%) of torticollis relapse in our study, in which the infants needed further
treatment in the outpatient clinic, demonstrate the importance of instructing
parents/caregivers to continue implementing the rehabilitation plan and to check head
posture after the post-discharge monitoring period.
Conclusions
By correctly assessing the motility and range of motion of the cervical spine, infants can be
prescribed the appropriate plan of care: a home or outpatient rehabilitation program.
It is important to discharge infants after full resolution of CMT symptoms has been
achieved and to actively encourage parents/caregivers to monitor neck posture in order to
exclude the minimal risk of relapse.
References
1. Stassen LFA, Kerawala CJ. New surgical technique for correction of congenital
muscular torticollis (wry neck). Br J Oral Maxillofac Surg 2000 Apr;; 38(2):142-7.
2. H
ollier L, Kim J. Congenital muscular torticollis and the associated craniofacial changes.
Plast Reconstr Surg 2000 Mar;; 105(3):827-35.
3. Cheng JCY, Au AWY . Infantile torticollis: a review of 624 cases. Journal of Pediatric
Orthopedics.1994 14:802-8.
4. Cheng JCY, Tang SP, Chen TMK, Wong MWN, Wong EMC. The clinical presentation
and outcome of treatment of congenital muscular torticollis in infants. A study of 1,086
cases. J Pediatr Surg. 2000 Jul;; 35 (7): 1091-6.
5. Bredenkamp JK, Hoover LA, Berke GS, Shaw A. Congenital muscular torticollis. A
spectrum of disease. Arch Otolaryngol Head Neck Surg 1990;;116:212-6.
6. Kaplan S, Coulter C, Fetters L. Physical therapy management of congenital muscular
torticollis: An evidence-based clinical practice guideline. Pediatr Phys Ther. 2013;;
25:(4):348–394.
7. Evidence-Based Care Guideline for Management of Congenital Muscular Torticollis in
children age 0 to 36 months. Cincinnati Children’s Hospital.
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http:/www.cincinnatichildrens.org/service/j/Anderson-center/evidence-based/care/raccoma
ndation/topic/. Accessed September 18, 2014.
8. Ballock RT and Song KM. The prevalence of nonmuscular causes of torticollis in
children. J pediatr Orthop 16:500, 1996.
9. Von Heideken J, Green DW, Burke SW, Sindle K, Denneen J, Haglund-Akerlind Y et al.
The Relationship Between Developmental Dysplasia of the Hip and Congenital Muscular
Torticollis. J Pediatr Orthop 2006;; 26: 805-808.
10. Walsh JJ, Morrissy RT. Torticollis and hip dislocation. J pediatr Orthop 1998;; 18:
219-221.
11. Wolfort FG, Kanter MA, Miller LB. Torticollis. Plastic and Reconstructive Surgery 1989
Oct;; 84(4):682-92.
12. Tufano RP, Tom LW, Austin MB. Bilateral sternocleidomastoid tumors of infancy. Int J
Pediatr Otorhinolaryngol. 1999 Nov 15;;51(1):41-5.
13. Sonmez K, Turkyilmaz Z, Demirogullari B, Ozen O, Karabulut R, Bagbanci B et al.
Congenital muscolar torticollis in children. ORL 2005;;67:344-347.
14. Tavill MA, Wetmore RF: A case of familial sternocleidomastoid tumors of infancy.
International J of Pediatric Otorhinolaryngology 38(1996) 163-68.
15. Tien YC, Su JY, Lin GT. Ultrasonographic Study of the Cohexistence of Muscular
Torticollis and Dysplasia of the hip. J pediatric Orthop 2001;; 21: 343-7.
16. Park HK, Kang EY, Lee SH, Kim KM, Jung AY, Nam DH. The utility of ultrasonography
for the diagnosis of developmental dysplasia of hip joint in congenital muscular torticollis.
Ann Rehab Med. 2013 Feb;;37(1):26-32.
17. Flannery AB, Looman WS, Kemper K. Evidence-Based Care of Child With
Deformational Phlagiocephaly, Part II: Management. J Pediatr Health Care. 2012
Sep-Oct;;26(5):320-31.
18. Stevens P, Downey C, Boyd V, Cole P, Stal S, Edmond J et al. Deformational
Plagiocephaly Associated with Ocular Torticollis: A Clinical Study and Literature Review.
The Journal of cranial surgery vol 18, N 2 March 2007.
19. Seo SJ, Yim SY ,Lee IJ. Is Craniofacial Asymmetry Progressive in Untreated
Congenital Muscular Torticollis. Volume 132(2), August 2013, p407-413).
20. Monson RM, Deitz J, Kartin D. The Relationship Between Awake Positioning and
Motor Performance Among Infants Who Slept Supine. Pediatr Phys Ther 2003;;
15:196-203.
21. Vernet O, de Ribaupierre S, Cavin B, Rilliet B. Treatment of posterior positional
plagiocephaly. Archives de Pediatrie 15 (2008) 1829-1833.
22. Ohman A, Nilsson S, Lagerkvist AL, Beckung E. Are infants with torticollis at risk of a
delay in early motor milestones compared with a control group of healthy infants? Dev
Med Child Neurol 2009 Jul;;51(7):545-50
23. Cheng JCY, Chen TMK, Tang SP, Shum SLF, Wong MWN, Metreweli C. Snapping
During Manual Stretching in Congenital Muscular Torticollis. Clin Orthop Rel Res 2001
Mar;; (384):237-44.
24. Wei JL, Schwartz KM, Weaver AL, Orvidas LJ. Pseudotumor of Infancy and
Congenital Muscular Torticollis: 170 Cases. Laryngoscope 111:688-695, 2001.
25. Cheng JCY, Wong MWN, Tang SP, Chen TMK, Shum SLF, Wong EMC. Clinical
determinants of the outcome of manual stretching in the treatment of congenital muscular
torticollis in infants. Journal of Bone and Joint Surg, 83: 679-87, 2001.
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26. Sudre-Levillain I, Nicollas R, Roman S, Aladio P,Moukheiber A, Triglia JM. The
sternocleidomastoid tumors of infancy. Archives de Pédiatrie Vol 7, Issue 11,Nov 2000,
1180-84.
27. Macdonald D. Sternomastoid tumor and muscular torticollis. J Bone Joint Surg [Br]
51-B:432-443, 1969.
28. Luther BL. Congenital muscular torticollis. Orthop Nurs. 2002 May-Jun;; 21 (3):21-7.
29. Davids JR, Wenger DR, Mubarak SJ. Congenital muscular torticollis: Sequela of
Intrauterine or Perinatal Compartment Syndrome. J Ped Orthop 13:141-147, 1993.
30. Yim SY, Yoon D, Park MC, Lee IJ, Kim JH, Lee MA et al. Integrative analysis of
congenital muscular torticollis: from gene expression to clinical significance. BMC Med
Genomics. 2013;; 6 Suppl 2:S10.
31. Lee SJ, Han JD,Lee HB, Hwang JH, Kim SY et al. Comparison of Clinical Severity of
Congenital Muscular Torticollis Based on the Method of Child Birth. Ann Rehabil Med
2011;;35:641-647.
32.Tatli B, Aydinli N, Cahskan M. Congenital muscular torticollis: evaluation and
classification. Pediatr Neurol 2006 Jan;; 34(1):41-4.
33. Bedi DG, John SD, Swischuk LE: Fibromatosis colli in infancy: variability of
sonographic appearance. Journal of clinical ultrasound 1997 Oct;; Vol 26 N 7.
34. Dudkiewicz I, Ganel A, Blankstein A: Congenital muscular torticollis in infants:
ultrasound-assisted diagnosis and evaluation. J Pediatr Orthop 2005;;25:812-14.
35. Tang SF, Hsu KH, Wong AM, Hsu CC, Chang CH. Longitudinal follow up study of
ultrasonography in congenital muscular torticollis. Clin Orthop Relat Res. 2002 Oct;;
(403):179-85.
36. Lin JN, Chou ML: Ultrasonographic study of sternocleidomastoid muscle in
management of congenital muscular torticollis. J Pediatr Surg.1997 Nov;; 32(11):1648-51.
37. Hsu TC, Wang CL, Wong MK, Hsu KH, Tang FT, Chen HT . Correlation of clinical and
ultrasonographic features in congenital muscular torticollis. Arch Phys Med Rehabil. 1999
Jun;;80(6):637-41.
38. Lehwald N, Krausch M, Franke C, Assmann B, Adam R, Knoefel WT. Sandifer
syndrome-a multidisciplinary diagnostic and therapeutic challenge. Eur J Pediatr Surg.
2007Jun;;17(3):203-6.
39. Halanski MA, Iskandar B, Nemeth B, Noonan KJ.:The coconut condyle: occipital
condylar dysplasia causing torticollis and leading to c1 fracture. J Spinal Disord Tech.
2006 Jun;;19(4):295-8.
40. Slate RK, Posnick JC, Armstrong DC, Buncic JR. Cervical spine subluxation
associated with congenital muscular torticollis and craniofacial asymmetry. Plast Reconstr
Surg 1993 Jun;;91(7):1187-95.
41. Do TT: Congenital muscular torticollis: current concepts and review of treatment. Curr
Opin in Pediatr. 2006 Feb;; 18(1):26-9.
42. Williams CRP, O’Flynn E, Clarke NMP, Morris RJ. Torticollis secondary to ocular
pathology. J Bone Joint Surg Br. 1996;;78:-B:620-4.
43. Goodman CR, Chabner E, and Guyton DL. Should early strabismus surgery be
performed for ocular torticollis to prevent facial asymmetry? J Pediatr Opthalmol
Strabismus 32: 162, 1995.
44. Petronic I, Brdar R, Cirociv D, Nikolic D, Lukac M, Janic D, Pavicevic P, Golubovic Z,
Knezevic T. Congenital muscular torticollis in children: distribution, treatment duration and
outcome Eur J Phys Rehabil Med. 2010 Jun;;46(2):153-7.
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45. Celayir AC. Congenital muscular torticollis: Early and intensive treatment is critical. A
prospective study. Pediatr Int. 2000;; 42:(5):504-507.
46. Joyce MB, Tristan de Chalain MB. Treatment of Recalcitrant Idiopathic Muscular
Torticollis in Infants with Botulinum Toxin Type A. J Craniofacial Surg. 2005
Mar;;16(2)321-27.
47. Canale ST, Griffin DW, Hubbard CN. Congenital muscular torticollis. J Bone Joint Surg
[Am] 64-A:810-816, 1982.
48. Shim JS, Jang HP. Operative treatment of congenital torticollis.J Bone and Joint Surg;;
2008 Jul;; 90, 7;; ProQuest Medical Library p 934.
49.Ohman A, Nilsson S, Beckung E. Stretching treatment for infants with congenital
muscular torticollis: physiotherapist or parents? A randomized pilot study. PM R. 2010
Dec;;2(12): 1073-9.
50. Demirbilek S, Atayurt HF. Congenital Muscular Torticollis and Sternomastoid Tumor:
Results of Nonoperative Treatment. Journal of Pediatric Surgery, Vol34, No 4 (April),
1999;; 549-551.
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