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12	 Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013
Review Article
Address for
correspondence:
Dr. M. Priyanka,
Department of
Periodontology, Meenakshi
Ammal Dental College,
Chennai, Tamil Nadu, India
E‑mail: priyanka13_28@
yahoo.com
Submission: 23‑02‑2011
Accepted: 01‑10‑2012
Department of
Periodontology,
Meenakshi Ammal
Dental College,
Chennai, Tamil Nadu,
India
An overview of frenal attachments
M. Priyanka, R. Sruthi, T. Ramakrishnan, Pamela Emmadi, N. Ambalavanan
Abstract:
Frenal attachments are thin folds of mucous membrane with enclosed muscle fibers that attach the lips to the
alveolar mucosa and underlying periosteum. Most often, during the oral examination of the patient the dentist
gives very little importance to the frenum, for assessing its morpholology and attachment. However, it has
been seen that an abnormal frenum can be an indicator of a syndrome. This paper highlights the different
frenal attachments seen in association with various syndromic as well as non‑syndromic conditions.
Key words:
Aberrant frena, frenulum, syndromes
INTRODUCTION
One of the more interesting yet often
misunderstood anatomic structures in the
oral cavity is the frenum‑ a mucosal attachment
of a loose part to a more rigid part.
A frenulum is a small frenum.[1]
There are several
frena that are usually present in a normal oral
cavity, most notably the maxillary labial frenum,
the mandibular labial frenum, and the lingual
frenum.
Theirprimaryfunctionistoprovidestabilityofthe
upper and lower lip and the tongue.[1]
The extent
of their involvement in mastication is in dispute.
Labial frenal attachments are thin folds of mucous
membranewithenclosedmusclefibersoriginating
fromorbicularisoris muscleofupperlipthatattach
at the lips to the alveolar mucosa and underlying
periosteum.[2]
It extends over the alveolar process
ininfantsandformsaraphethatreachesthepalatal
papilla. Through the growth of alveolar process as
the teeth erupt, this attachment generally changes
to assume the adult configuration.
CLASSIFICATION
Depending upon the extension of attachment of
fibers, frena have been classified as:[3]
1.	Mucosal – when the frenal fibers are attached
up to mucogingival junction [Figure 1]
2.	 Gingival – when fibres are inserted within
attached gingiva [Figure 2]
3.	 Papillary – when fibres are extending into
inter dental papilla; [Figure 3] and
4.	 Papilla penetrating – when the frenal fibres
cross the alveolar process and extend up to
palatine papilla [Figure 4].
Other variations of normal frenal attachment
include:[4]
•	 Simple frenum with anodule [Figure 5]
•	 Simple frenum with appendix [Figure 6]
•	 Simple frenum with nichum [Figure 7]
•	 Bifid labial frenum
•	 Persistent tectolabial frenum
•	 Double frenum
•	 Wider frenum [Figure 8]
Abnormal or aberrant frena are detected visually,
by applying tension over it to see the movement
of papillary tip or blanching produced due to
ischemia of the region. Clinically, papillary
and papilla penetrating frena are considered as
pathologicalandhavebeenfoundtobeassociated
with loss of papilla, recession, diastema, difficulty
in brushing, malalignment of teeth and it may
also prejudice the denture fit or retention leading
to psychological disturbances to the individual.[5]
A frenum can become a significant problem if
tension from lip movement pulls the gingival
margin away from the tooth, or if the tissue
inhibits the closure of a diastema during
orthodontic treatment.
Frenal attachment that encroach on the marginal
gingiva distend the gingival sulcus, fostering
plaque accumulation, increasing the rate of
progression of periodontal recession and thereby
leading to recurrence after treatment.
Syndromes associated with different frenal
attachments:
•	 Ehlers‑Danlos syndrome
•	 Infantile hypertrophic pyloric stenosis,
•	 Holoprosencephaly,
•	 Ellis‑van Creveld syndrome, and
•	 Oro‑facial‑digital syndrome.
Each syndrome exhibits relatively specific frenal
abnormalities, ranging from multiple, hyper
plastic, hypoplastic, or an absence of frena.
Access this article online
Website:
www.jisponline.com
DOI:
10.4103/0972-124X.107467
Quick Response Code:
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Priyanka, et al.: Frenal attachments
Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013	 13
Figure 1: Mucosal frenal attachment Figure 2: Gingival frenal attachment
Figure 3: Papillary frenal attachment Figure 4: Papilla penetrating frenal attachment
Figure 5: Simple frenum with a nodule Figure 6: Simple frenum with appendix
Figure 7: Simple frenum with nichum Figure 8: Wider frenal attachment
[Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]
Priyanka, et al.: Frenal attachments
14	 Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013
Oro‑facial-digital syndrome
Oro-facial-digital syndrome arises as the result of a single
gene malformation showing X‑linked dominant inheritance.[6]
Clinical features within the oral cavity:
•	 The tongue is lobulated with hamartomata between lobules,
hypertrophied lingual frenum which is incompletely
differentiated from the floor of the mouth
•	 Gums are clefted by abnormal supernumerary frenula
•	 Cleft often in soft palate, might be bilateral or asymmetrical
•	 Teeth are malpositioned, often and may have enamel
hypoplasia
•	 Midline notch (pseudocleft) may be seen in the upper lip.
Infantile hypertrophic pyloric stenosis
Occurs commonly in males at a ratio of 4.5 to 1 with an unknown
etiology. There is a disturbance in the frenum formation.
The absence or hypoplasia of mandibular frenum represents an
important diagnostic tool in detection of this disease.[7]
Holoprosencephaly
It is an autosomal dominant condition characterized by a brain
malformationduetodefectsinprosencephalon.Itischaracterized
by defects including cyclopia, single nostril, single central incisor
and premaxillary agenesis. Absence of labial maxillary frenum is
one of the characteristic features of this condition.[8]
Ellis‑van Creveld syndrome
Ellis‑van Creveld (EvC) syndrome is an autosomal recessive
disorder, mainly affecting the ectodermal components such
as enamel, nail, and hair. The gene for EvC syndrome is
located on chromosome 4p16. Patients with EvC syndrome
characteristically presents with congenitally missing teeth,
abnormal frenal attachment, microdontia, and hexadactyly.[9]
Oral manifestations in the EvC syndrome are characteristic and
constant. The most constant finding is fusion of the anterior
portion of the upper lip to the maxillary gingival margin, as a
result of which no mucobuccal fold exists, causing the upper
lip to present a slight V‑shaped notch in the middle. Changes
in the upper lip can be addressed by various names such as
partial hare‑lip or lip tie. The anterior portion of the lower ridge
is often serrated and presents with multiple small labial frenula.
The maxillary and mandibular alveolar process presents with
notching or submucous clefts and continuous or broad labial
frenula with dystrophic philtrum.[9]
Ehlerdanlos syndrome
It is a genetic disorder characterized by hyper extensive skin
and hyper mobile joints with no gender predilection. Absence
of the inferior labial and lingual frena has been described in
this disorder.[10]
Pallister‑hall syndrome
Inherited as an autosomal dominant pattern. The gene
responsible for this disorder has been mapped to 7p13 and
is identified as GL13.Clinical features include short mid face
and nose with a flat nasal bridge and anteverted nostrils.
Oral manifestations include micrognathia, microglossia and
abnormal supernumerary frena extending from the buccal
mucosa to the alveolar ridge.[11]
Opitz C syndrome
Exhibits similar frenal abnormalities as Pallister‑Hall
syndrome.[12]
Nonsyndromic conditions
In addition to abnormal oral frena observed in syndromic
conditions, anomalous frena are encountered without other
associated phenotypic features of genetic or chromosomal
states. For example ankylosis of superior labial frena may show
a familiar pattern of occurrence.[1]
Aberrant frenal attachments may be seen after orthognathic
surgeries. Problems are probably caused by errors in the
surgical technique. The design of the soft tissue incisions
is critical, vertical incisions in the area of osteotomy will
predictably create periodontal problems.[13]
MANAGEMENT
Three surgical techniques are effective in removal of frenal
attachments
1.	 The simple excision technique
2.	 The Z‑plasty technique
3.	 Alocalizedvestibuloplastywithsecondaryepithelialization.
The first two techniques are effective when the mucosal
and fibrous tissue band is relatively narrow; the third
technique is often preferred when the frenal attachment
has a wide base.
Simple excision technique
•	 A narrow elliptic incision around the frenal area down to
the periosteum is given
•	 The fibrous frenum is then sharply dissected from the
underlying periosteum and soft tissue, and the margins of
the wound are gently undermined and re‑approximated.
Z‑plasty technique
•	 After excision of the fibrous tissue, two oblique incisions
are made in a Z fashion, one at each end of the previous
area of excision
•	 Two pointed flaps are then gently undermined and rotated
to close the initial vertical incision horizontally.
Localized vestibuloplasty with secondary epithelialization:
•	 An incision is made through mucosal tissue and underlying
submucosal tissue, without perforating the periosteum
•	 A supraperiosteal dissection is completed by undermining
the mucosal and submucosal tissue with scissors
•	 After a clean periosteal layer is identified, the edge of the
mucosal flap is sutured to the periosteum at the maximal
depth of the vestibule and the exposed periosteum is
allowed to heal by secondary epithelialization.
CONCLUSION
Frenum may not regularly draw close scrutiny on routine dental
examination. However, the detection of abnormal frenum
may represent a highly useful indicator in the diagnosis of
a wide array of syndromic and non‑syndromic conditions.
However, the presence of any abnormal frenal attachments
[Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]
Priyanka, et al.: Frenal attachments
Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013	 15
can be corrected with a wide variety of surgical techniques
available.
REFERENCES
1.	 Mintz SM, Siegel MA, Seider PJ. An overview of oral
frena and their association with multiple syndromes and
nonsyndromic conditions. Oral Surg Oral Med Oral Pathol Oral
RadiolEndod2005;99:321‑4.
2.	 Kotlow LA. Oral diagnosis of abnormal frenum attachments
in neonates and infants: Evaluation and treatment of maxillary
frenum using the Erbium YAG Laser. J Pediatr Dent Care 2004c;
10:11‑4
3.	 Mirko P, Miroslav S, Lubor M. Significance of the labial frenum
attachment in periodontal disease in man. Part I. Classification
and epidemiology of the labial frenum attachment. J Periodontol
1974;45:891‑4.
4.	 Kakodkar PV, Patel TN, Patel SV, Patel SH. Clinical assessment
of diverse frenum morphology in Permanent dentition. Internet
J Dent Sci 2009;7.
5.	 Anubha  N, Chaubey KK, AroraVK, Narula IS. Frenectomy
combined with a laterally displaced pedicle graft. Indian J Dent
Sci 2010;2:47‑51.
6.	 Dodge JA, Kernohan DC. Oral facial digital syndrome. Arch Dis
Child 1967;42:214‑9.
7.	 Jenista JA. Madibular frenulum as a sign of infantile hypertrophic
pyloric stenosis. J Pediatr 2001;138:447.7.
8.	 Martin RA, Jones KL. Absence of the superior labial frenulum
in holoprosencephaly: A new diagnostic sign. J Pediatr
1998;133:151‑3.
9.	 Babaji P. Oral abnormalities in the Ellis‑van creveldsyndrome.
Indian J Dent Res 2010;21:143‑5.
10.	 De Felice C, Toti P, Di Maggio G, Parinni S, Bagnoli F. Absence of
the inferior labial and lingual frenula in Ehlers‑Danlos syndrome.
Lancet 2001;357:1500‑2.10.
11.	 Hall JG, Pallister PD, Clarren SK, Beck with JB. Congenital
hypothalamic hamartoblastoma, hypopituitarism, imperforate
anus and postaxial polydactyly: A new syndrome? Part I:
Clinical, causal and pathogenic considerations. Am J Med Genet
1980;7:47‑74.
12.	 Brooks JK, Leonard CO, Coccaro PJ Jr. (Opitz (BBG/G) syndrome:
Oral manifestations. Am J Med Genet 1992;43:595‑601.
13.	 Panula K, Finne K, Oikarinen K. Incidence of complications
and problems related to orthognathic surgery: A review of
655 patients. J Oral MaxillofacSurg 2001;59:1128‑36.
“Quick Response Code” link for full text articles
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How to cite this article: Priyanka M, Sruthi R, Ramakrishnan T,
Emmadi P, Ambalavanan N. An overview of frenal attachments. J
Indian Soc Periodontol 2013;17:12-5.
Source of Support: Nil, Conflict of Interest: None declared.
[Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]

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Co-Existence of Synodontia & Talon Cusp in Mandible: A Rare Case
 

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JIndianSocPeriodontol17112-6038587_164625.pdf

  • 1. 12 Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013 Review Article Address for correspondence: Dr. M. Priyanka, Department of Periodontology, Meenakshi Ammal Dental College, Chennai, Tamil Nadu, India E‑mail: priyanka13_28@ yahoo.com Submission: 23‑02‑2011 Accepted: 01‑10‑2012 Department of Periodontology, Meenakshi Ammal Dental College, Chennai, Tamil Nadu, India An overview of frenal attachments M. Priyanka, R. Sruthi, T. Ramakrishnan, Pamela Emmadi, N. Ambalavanan Abstract: Frenal attachments are thin folds of mucous membrane with enclosed muscle fibers that attach the lips to the alveolar mucosa and underlying periosteum. Most often, during the oral examination of the patient the dentist gives very little importance to the frenum, for assessing its morpholology and attachment. However, it has been seen that an abnormal frenum can be an indicator of a syndrome. This paper highlights the different frenal attachments seen in association with various syndromic as well as non‑syndromic conditions. Key words: Aberrant frena, frenulum, syndromes INTRODUCTION One of the more interesting yet often misunderstood anatomic structures in the oral cavity is the frenum‑ a mucosal attachment of a loose part to a more rigid part. A frenulum is a small frenum.[1] There are several frena that are usually present in a normal oral cavity, most notably the maxillary labial frenum, the mandibular labial frenum, and the lingual frenum. Theirprimaryfunctionistoprovidestabilityofthe upper and lower lip and the tongue.[1] The extent of their involvement in mastication is in dispute. Labial frenal attachments are thin folds of mucous membranewithenclosedmusclefibersoriginating fromorbicularisoris muscleofupperlipthatattach at the lips to the alveolar mucosa and underlying periosteum.[2] It extends over the alveolar process ininfantsandformsaraphethatreachesthepalatal papilla. Through the growth of alveolar process as the teeth erupt, this attachment generally changes to assume the adult configuration. CLASSIFICATION Depending upon the extension of attachment of fibers, frena have been classified as:[3] 1. Mucosal – when the frenal fibers are attached up to mucogingival junction [Figure 1] 2. Gingival – when fibres are inserted within attached gingiva [Figure 2] 3. Papillary – when fibres are extending into inter dental papilla; [Figure 3] and 4. Papilla penetrating – when the frenal fibres cross the alveolar process and extend up to palatine papilla [Figure 4]. Other variations of normal frenal attachment include:[4] • Simple frenum with anodule [Figure 5] • Simple frenum with appendix [Figure 6] • Simple frenum with nichum [Figure 7] • Bifid labial frenum • Persistent tectolabial frenum • Double frenum • Wider frenum [Figure 8] Abnormal or aberrant frena are detected visually, by applying tension over it to see the movement of papillary tip or blanching produced due to ischemia of the region. Clinically, papillary and papilla penetrating frena are considered as pathologicalandhavebeenfoundtobeassociated with loss of papilla, recession, diastema, difficulty in brushing, malalignment of teeth and it may also prejudice the denture fit or retention leading to psychological disturbances to the individual.[5] A frenum can become a significant problem if tension from lip movement pulls the gingival margin away from the tooth, or if the tissue inhibits the closure of a diastema during orthodontic treatment. Frenal attachment that encroach on the marginal gingiva distend the gingival sulcus, fostering plaque accumulation, increasing the rate of progression of periodontal recession and thereby leading to recurrence after treatment. Syndromes associated with different frenal attachments: • Ehlers‑Danlos syndrome • Infantile hypertrophic pyloric stenosis, • Holoprosencephaly, • Ellis‑van Creveld syndrome, and • Oro‑facial‑digital syndrome. Each syndrome exhibits relatively specific frenal abnormalities, ranging from multiple, hyper plastic, hypoplastic, or an absence of frena. Access this article online Website: www.jisponline.com DOI: 10.4103/0972-124X.107467 Quick Response Code: [Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]
  • 2. Priyanka, et al.: Frenal attachments Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013 13 Figure 1: Mucosal frenal attachment Figure 2: Gingival frenal attachment Figure 3: Papillary frenal attachment Figure 4: Papilla penetrating frenal attachment Figure 5: Simple frenum with a nodule Figure 6: Simple frenum with appendix Figure 7: Simple frenum with nichum Figure 8: Wider frenal attachment [Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]
  • 3. Priyanka, et al.: Frenal attachments 14 Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013 Oro‑facial-digital syndrome Oro-facial-digital syndrome arises as the result of a single gene malformation showing X‑linked dominant inheritance.[6] Clinical features within the oral cavity: • The tongue is lobulated with hamartomata between lobules, hypertrophied lingual frenum which is incompletely differentiated from the floor of the mouth • Gums are clefted by abnormal supernumerary frenula • Cleft often in soft palate, might be bilateral or asymmetrical • Teeth are malpositioned, often and may have enamel hypoplasia • Midline notch (pseudocleft) may be seen in the upper lip. Infantile hypertrophic pyloric stenosis Occurs commonly in males at a ratio of 4.5 to 1 with an unknown etiology. There is a disturbance in the frenum formation. The absence or hypoplasia of mandibular frenum represents an important diagnostic tool in detection of this disease.[7] Holoprosencephaly It is an autosomal dominant condition characterized by a brain malformationduetodefectsinprosencephalon.Itischaracterized by defects including cyclopia, single nostril, single central incisor and premaxillary agenesis. Absence of labial maxillary frenum is one of the characteristic features of this condition.[8] Ellis‑van Creveld syndrome Ellis‑van Creveld (EvC) syndrome is an autosomal recessive disorder, mainly affecting the ectodermal components such as enamel, nail, and hair. The gene for EvC syndrome is located on chromosome 4p16. Patients with EvC syndrome characteristically presents with congenitally missing teeth, abnormal frenal attachment, microdontia, and hexadactyly.[9] Oral manifestations in the EvC syndrome are characteristic and constant. The most constant finding is fusion of the anterior portion of the upper lip to the maxillary gingival margin, as a result of which no mucobuccal fold exists, causing the upper lip to present a slight V‑shaped notch in the middle. Changes in the upper lip can be addressed by various names such as partial hare‑lip or lip tie. The anterior portion of the lower ridge is often serrated and presents with multiple small labial frenula. The maxillary and mandibular alveolar process presents with notching or submucous clefts and continuous or broad labial frenula with dystrophic philtrum.[9] Ehlerdanlos syndrome It is a genetic disorder characterized by hyper extensive skin and hyper mobile joints with no gender predilection. Absence of the inferior labial and lingual frena has been described in this disorder.[10] Pallister‑hall syndrome Inherited as an autosomal dominant pattern. The gene responsible for this disorder has been mapped to 7p13 and is identified as GL13.Clinical features include short mid face and nose with a flat nasal bridge and anteverted nostrils. Oral manifestations include micrognathia, microglossia and abnormal supernumerary frena extending from the buccal mucosa to the alveolar ridge.[11] Opitz C syndrome Exhibits similar frenal abnormalities as Pallister‑Hall syndrome.[12] Nonsyndromic conditions In addition to abnormal oral frena observed in syndromic conditions, anomalous frena are encountered without other associated phenotypic features of genetic or chromosomal states. For example ankylosis of superior labial frena may show a familiar pattern of occurrence.[1] Aberrant frenal attachments may be seen after orthognathic surgeries. Problems are probably caused by errors in the surgical technique. The design of the soft tissue incisions is critical, vertical incisions in the area of osteotomy will predictably create periodontal problems.[13] MANAGEMENT Three surgical techniques are effective in removal of frenal attachments 1. The simple excision technique 2. The Z‑plasty technique 3. Alocalizedvestibuloplastywithsecondaryepithelialization. The first two techniques are effective when the mucosal and fibrous tissue band is relatively narrow; the third technique is often preferred when the frenal attachment has a wide base. Simple excision technique • A narrow elliptic incision around the frenal area down to the periosteum is given • The fibrous frenum is then sharply dissected from the underlying periosteum and soft tissue, and the margins of the wound are gently undermined and re‑approximated. Z‑plasty technique • After excision of the fibrous tissue, two oblique incisions are made in a Z fashion, one at each end of the previous area of excision • Two pointed flaps are then gently undermined and rotated to close the initial vertical incision horizontally. Localized vestibuloplasty with secondary epithelialization: • An incision is made through mucosal tissue and underlying submucosal tissue, without perforating the periosteum • A supraperiosteal dissection is completed by undermining the mucosal and submucosal tissue with scissors • After a clean periosteal layer is identified, the edge of the mucosal flap is sutured to the periosteum at the maximal depth of the vestibule and the exposed periosteum is allowed to heal by secondary epithelialization. CONCLUSION Frenum may not regularly draw close scrutiny on routine dental examination. However, the detection of abnormal frenum may represent a highly useful indicator in the diagnosis of a wide array of syndromic and non‑syndromic conditions. However, the presence of any abnormal frenal attachments [Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]
  • 4. Priyanka, et al.: Frenal attachments Journal of Indian Society of Periodontology - Vol 17, Issue 1, Jan-Feb 2013 15 can be corrected with a wide variety of surgical techniques available. REFERENCES 1. Mintz SM, Siegel MA, Seider PJ. An overview of oral frena and their association with multiple syndromes and nonsyndromic conditions. Oral Surg Oral Med Oral Pathol Oral RadiolEndod2005;99:321‑4. 2. Kotlow LA. Oral diagnosis of abnormal frenum attachments in neonates and infants: Evaluation and treatment of maxillary frenum using the Erbium YAG Laser. J Pediatr Dent Care 2004c; 10:11‑4 3. Mirko P, Miroslav S, Lubor M. Significance of the labial frenum attachment in periodontal disease in man. Part I. Classification and epidemiology of the labial frenum attachment. J Periodontol 1974;45:891‑4. 4. Kakodkar PV, Patel TN, Patel SV, Patel SH. Clinical assessment of diverse frenum morphology in Permanent dentition. Internet J Dent Sci 2009;7. 5. Anubha  N, Chaubey KK, AroraVK, Narula IS. Frenectomy combined with a laterally displaced pedicle graft. Indian J Dent Sci 2010;2:47‑51. 6. Dodge JA, Kernohan DC. Oral facial digital syndrome. Arch Dis Child 1967;42:214‑9. 7. Jenista JA. Madibular frenulum as a sign of infantile hypertrophic pyloric stenosis. J Pediatr 2001;138:447.7. 8. Martin RA, Jones KL. Absence of the superior labial frenulum in holoprosencephaly: A new diagnostic sign. J Pediatr 1998;133:151‑3. 9. Babaji P. Oral abnormalities in the Ellis‑van creveldsyndrome. Indian J Dent Res 2010;21:143‑5. 10. De Felice C, Toti P, Di Maggio G, Parinni S, Bagnoli F. Absence of the inferior labial and lingual frenula in Ehlers‑Danlos syndrome. Lancet 2001;357:1500‑2.10. 11. Hall JG, Pallister PD, Clarren SK, Beck with JB. Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly: A new syndrome? Part I: Clinical, causal and pathogenic considerations. Am J Med Genet 1980;7:47‑74. 12. Brooks JK, Leonard CO, Coccaro PJ Jr. (Opitz (BBG/G) syndrome: Oral manifestations. Am J Med Genet 1992;43:595‑601. 13. Panula K, Finne K, Oikarinen K. Incidence of complications and problems related to orthognathic surgery: A review of 655 patients. J Oral MaxillofacSurg 2001;59:1128‑36. “Quick Response Code” link for full text articles The journal issue has a unique new feature for reaching to the journal’s website without typing a single letter. Each article on its first page has a “Quick Response Code”. Using any mobile or other hand-held device with camera and GPRS/other internet source, one can reach to the full text of that particular article on the journal’s website. Start a QR-code reading software (see list of free applications from http://tinyurl.com/ yzlh2tc) and point the camera to the QR-code printed in the journal. It will automatically take you to the HTML full text of that article. One can also use a desktop or laptop with web camera for similar functionality. See http://tinyurl.com/2bw7fn3 or http://tinyurl.com/3ysr3me for the free applications. How to cite this article: Priyanka M, Sruthi R, Ramakrishnan T, Emmadi P, Ambalavanan N. An overview of frenal attachments. J Indian Soc Periodontol 2013;17:12-5. Source of Support: Nil, Conflict of Interest: None declared. [Downloaded free from http://www.jisponline.com on Thursday, March 17, 2022, IP: 252.212.241.118]