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 Table of Contents  
CASE REPORT
Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 103-106  

Hereditary sensory and autonomic neuropathy type V: Report of a rare case


1 Department of Pedodontics, Government Dental College and Hospital, Nagpur, Maharashtra, India
2 Department of Oral Medicine and Radiology, VSPM Dental College and Research Centre, Nagpur, Maharashtra, India

Date of Web Publication14-Jan-2015

Correspondence Address:
Ritesh Kalaskar
Department of Pedodontics, Government Dental College and Hospital, Nagpur, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0976-237X.149302

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   Abstract 

Hereditary sensory and autonomic neuropathy (HSAN) type V is a rare inherited disease caused by a mutation in the neurotrophic tyrosine kinase receptor, type 1 gene located on chromosome 1 (1q21-q22). It is characterized by pain insensitivity, partial anhydrosis without mental retardation and unimpaired touch and pressure sensitivity. Self-mutilation injury involving the teeth, lips, tongue, ears, eyes, nose, and fingers are invariable feature of this disorder. The purpose of this paper was to discuss the diagnosis and oral management of 18-month-old girl with HSAN type V, having typical oral manifestation of bitten tongue and auto-extraction of primary teeth. Modified bite guard was given to the patient to prevent further self-mutilating injuries to the tongue.

Keywords: Auto-extraction, bite guard, bitten tongue, hereditary sensory and autonomic neuropathies, insensitivity to pain


How to cite this article:
Kalaskar R, Kalaskar A. Hereditary sensory and autonomic neuropathy type V: Report of a rare case. Contemp Clin Dent 2015;6:103-6

How to cite this URL:
Kalaskar R, Kalaskar A. Hereditary sensory and autonomic neuropathy type V: Report of a rare case. Contemp Clin Dent [serial online] 2015 [cited 2019 Jul 17];6:103-6. Available from: http://www.contempclindent.org/text.asp?2015/6/1/103/149302


   Introduction Top


Hereditary sensory and autonomic neuropathies (HSAN) encompass a number of inherited disorders that are associated with sensory and varying degrees of autonomic dysfunction. [1] Until date, HSAN has been classified into five types: type I is autosomal dominant whereas types II, III, IV, and V are autosomal recessive. [1]

Type I is a relatively mild condition, manifested in the second to fourth decade mainly affecting the lower limbs. Type II is also associated with loss of sweating but temperature and control of blood pressure are normal. Type III has a multisystem presentation including postural hypotension, ataxia, kyphoscoliosis, oropharyngeal dyscordination, and abnormal gastro-esophageal motility resulting in feeding difficulties and recurrent aspiration pneumonia. Type IV is manifested in infancy and is associated with pain insensitivity, complete anhydrosis, mental retardation and self-mutation. Type V disease is similar to type IV, but is relatively mild without mental retardation and less sevier anhydrosis. [2]

Hereditary sensory and autonomic neuropathy type V is characterized by lack of pain perception, mentally sound and partial anhydrosis, but with preservation of all other sensory modalities, including normal touch perception, proprioception, itch, warm and cold temperature discrimination and vibration (OMIM 608654). [3],[4] It is caused by a mutation in the neurotrophic tyrosine kinase receptor, type 1 (NTRK1) gene located on chromosome 1 (1q21-q22), coding for nerve growth factor beta (NGFB) gene. [3],[5] The loss of pain sensation interferes with body protective mechanism, sleep, mobility, nutrition, thoughts, sexual activity, emotional well-being, creativity, and self-actualization. Self-mutilation is an almost invariable feature of this disorder, most often involving the teeth, lips, tongue, ears, eyes, nose, and fingers. [4] Bone fractures are also asymptomatic and affected individuals are not aware of these fractures until a limp develops. [5] This is an extremely dangerous disorder, but people can live a fairly normal life, provided, they constantly monitor for their cuts, bruises, self-mutilations and other possible unfelt injuries. This clinical report outlines a classical case of rare HSAN type V from central India highlighting the management of self-mutation to teeth and tongue. The report will also assist the oral health care providers in diagnosing the disorder and timely referral of such patients to the appropriate health care professionals .


   Case Report Top


An 18-month-old girl, born to a healthy nonconsanguineous couple, was brought to our department for the management of self-mutilated biting of the tongue. She had normal milestones since birth. At the age of 7 months, her parents first notice that she did not respond to painful stimuli like injection of vaccines or any other accidental trauma. She had a history of heat intolerance, reduced sweating and fewer tears while crying. She had no history of recurrent fever, poor vision, seizure, skin rash, and bleeding manifestation. Parents gave history of biting of the tongue (since the eruption of teeth), grinding of teeth and repeated attempts to remove the teeth with fingers. Her taste sensation was normal. Pregnancy and birth were uneventful. There was no family history of neurologic or metabolic disorders, and no other member of their family was diagnosed with HSAN. On general examination, no signs of pallor, cyanosis, and icterus were observed. Hematological and biochemical investigations including serum uric acid levels were normal. Intraoral examination revealed self-mutilated features such as bitten tongue (resection of anterior one third of the tongue), ulceration on the ventral surface of tongue and auto-extraction of primary mandibular right and left central and lateral incisors and left canine. Primary maxillary right and left canines were un-erupted [Figure 1] and [Figure 2]. Cutaneous examination did not reveal generalized xerosis over ankles and dorsa of feet, thickening of palms, and fissuring of soles [Figure 3]. Sensory examination showed complete loss of pain and temperature sensations, but fine touch and vibration were preserved. Tendon reflexes and plantar responses were normal. Histological examination of the skin showed normal epidermal and dermal structures, including presence of normal sweat glands. Due to lack of availability of genetic tests, mutational study could not be done. Also, patient's parents were not ready for nerve biopsy because of invasiveness and nonfeasibility of the procedure. Based on the clinical findings, degree of both sensory and autonomic dysfunction, biochemical evaluations and skin histological features the probable diagnosis of HSAN type V was made. The parents were explained the importance of the remaining tongue and various treatment options. Patient parent did not agree for full mouth extraction of teeth because of the psychological and functional implications. Then, it was decided to give bite guard to prevent self-mutilated trauma to the tongue. Maxillary and mandibular jaw impressions were recorded in alginate and casts were made in die stone. Bite guard was prepared from biocryl X sheet, (Grate Lakes Orthodontics, Tonawanda, NY, USA) using Ministar pressure forming machine (Grate Lakes Orthodontics, Tonawanda, NY, USA). Bite guard was modified in such a way that it covered the palatal surface [Figure 4]a and b.
Figure 1: Intraoral photograph bitten tongue and autoextraction of 73, 72, 71, 81, and 82

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Figure 2: Photograph of maxillary and mandibular casts showing primary teeth

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Figure 3: Photograph hand and feet showing no cutaneous abnormality

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Figure 4: (a) Extraoral photograph of bite guard. (b) Intraoral photograph showing modifi ed bite guard

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Patient's parents were advised to remove the bite guard at an interval of 2-3 h. Patient was recalled weekly. After 1 month, there was no fresh episode of tongue biting. As the patient was too small to understand the importance of tongue and teeth, the bite guard was continued, and the parents were advice to report at 3 months interval. The parents were also advice for the regular visit to their physician, so that cuts, bruises, self-mutilations, any insensitive internal problems and other possible injuries are not un-left unattended.

During 8 months follow-up period, she had a history of trauma, which resulting in an avulsion of primary maxillary right central incisor and primary mandibular right canine. Primary maxillary right and left canines were erupted [Figure 5]a. After a follow-up of 9 months, bite guard was discontinued as it was loose, and there was no fresh episode of tongue biting. Twelve months follow-up showed complete healing of tongue and there was no episode of self-mutilated injury to oral structures [Figure 5]b. The patient is on regular follow-up at 3 monthly intervals.
Figure 5: (a) Intraoral photograph showing erupted 53, 63 and avulsed 52. (b) Twelve months intraoral photograph

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   Discussion Top


The presentation of congenital disorder and syndromic children in the dental office is a great challenge to the oral health care providers. Various congenital disorders are identified early in infancy and demand special attention right from birth. Type V HSAN is a congenital disorder with pain insensitivity can be diagnosed just after birth. Insensitivity to pain is also a characteristic feature of HSAN type IV, which is caused by the mutation in the NTRK1 gene located on chromosome 1 (1q21-q22), which codes for the NGF receptor, TrkA. [5],[6] The above two congenital neuropathies can be differentiated on the basis of two clinical features and also nerve biopsy. Greater severity of anhydrosis is present in HSAN type IV compared with HSAN type V. Mental retardation is not seen in patients with HSAN type V, which is a feature that is always present in HSAN type IV. [6],[7],[8] In HSAN type V, severe reduction of unmyelinated nerve fibers and a moderate loss of thin myelinated nerve fibers is present, whereas HSAN type IV patients' show reduced small myelinated nerve fibers and normal large myelinated nerve fibers. [9],[10]

Impairment of pain sensation and self-mutilation may also be seen in rare syndromes such as Lesch-Nyhan syndrome and de Lange syndrome. [11] Type V HSAN can be differentiated from these syndromes by the presence of partial anhydrosis, absence of peripheral nerve thickening and dysmorphic features, a normal serum uric acid level and electrophysiological studies and histopathological findings of nerve fiber loss. [11]

Comprehensive literature search has revealed limited reports on HSAN type V. Till date only one epidemiological survey has been conducted on HSAN types IV and V in Japan in which questionnaires reported from 105 institutes were evaluated. The survey estimated that the number of Japanese patients with HSAN types IV and V were 130-210 and 30-60 patients respectively. [12] Similarly, in 2004, a Swedish family, suffering from pain insensitivity underwent identification of a mutation in the NGFB gene responsible for pain sensation. [6] They found severe reduction of unmyelinated nerve fibers and a moderate loss of thin myelinated nerve fibers which confirmed the diagnosis of HSAN type V. In the present case report, genetic test and nerve biopsy was not possible; therefore, the diagnosis was made on the basis of classical clinical features: the degree of both sensory and autonomic dysfunction and biochemical evaluations. Thus, the oral health care provider should be aware of other investigations to differentiate these neuropathies.

There is no standard formula for the treatment of type V HSAN. Medical management is supportive and oriented to control the hyperthermia, prevention of self-mutilation and treatment of orthopedic problems. To avoid hyperthermia excessive wrapping is advocated, dehydration is prevented by acetaminophen and/or ibuprofen or by direct cooling in a bath or in a cooling blanket. Chlorpromazine or chloral hydrate is also effective in relaxing children and allowing them to cool. [1] The patient should be continuously monitored for cuts, bruises, burns, fractures, corneal ulceration, self-mutilations, so that wounds can be treated on time to prevent the spread of infection. For orthopedic complications use of special footwear, periods of nonweight-bearing are advocated. Patients with osteomyelitis can undergo surgery such as osteotomy and amputation. [1]

Typical oral manifestations in HSAN type V are ulcers on the ventral surface of the tongue due to repeated biting during infancy (resection of anterior portion of tongue), auto-extraction of the teeth and tearing wounds mostly on the lower lip. [3],[8] Oral management of these patients should focus on preventing injury to the tongue, lips, teeth, and oral mucosa. Children will require grinding of the teeth or extraction of all teeth or bite guard to prevent self-mutilation injury to the tongue and lips. Bite guard is preferred over the other options because: it not only prevents trauma to the tongue, but also maintains jaw relation, alveolar height, esthetic, helps in speech and mastication. Majority of reports in the literature with this disorder have advocated bite guard, but none of them had actually given it to the patient. In the present case, we have given a modified form of the bite guard that is easy to insert and remove and prevents swallowing or choking into the pharynx. Extraction of all the teeth should be avoided because that will have a psychological impact on children and might contribute to hyperthermia. If extraction of all teeth is planned, it should be done under local anesthesia to prevent undue tactile discomfort postoperatively. [13],[14] Some authors have described the difference in concentrations of inhaled anesthetics needed for orthopedic surgery and dental surgery. They speculated that these differences were caused by the nociceptive stimulus of each operation. [14],[15] Preventive dental care such as pit and fissure sealants, oral prophylaxis and professional topical fluoride application must be done. Parents should be made aware about the consequences of the dental caries particularly in relation to absence of pain.

Type V HASN is extremely dangerous and in most of the cases the patient does not live over the age of 25. [8] But with the understanding of this disorder and with helping patient to achieve independent function with minimal physical limitations we can increase the life of these patients. Further prognosis will be based on increased understanding of specific gene actions that will lead to definitive therapies.


   Conclusion Top


Diagnosis and management of HSAN type V is a great challenge to the oral health care provider. A rare case of HSAN type V, showing the usual features of bitten tongue was managed by a modified bite guard. Although genetic disorders affecting the sensory and autonomic nervous systems are rare, their existence provides a means of furthering our knowledge regarding a very complex part of the nervous system.

 
   References Top

1.
Axelrod FB, Gold-von Simson G. Hereditary sensory and autonomic neuropathies: Types II, III, and IV. Orphanet J Rare Dis 2007;2:39.  Back to cited text no. 1
    
2.
Sasnur AH, Sasnur PA, Ghaus-Ul RS. Congenital insensitivity to pain and anhidrosis. Indian J Orthop 2011;45:269-71.  Back to cited text no. 2
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3.
Houlden H, King RH, Hashemi-Nejad A, Wood NW, Mathias CJ, Reilly M, et al. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Ann Neurol 2001;49:521-5.  Back to cited text no. 3
    
4.
Online Mendelian Inheritance in Man. An online catalog of human genes and genetic disorder. Available from: http://www.omim.org/119530 [Last accessed on 2014 Oct 12].  Back to cited text no. 4
    
5.
Carvalho OP, Thornton GK, Hertecant J, Houlden H, Nicholas AK, Cox JJ, et al. A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy. J Med Genet 2011;48:131-5.  Back to cited text no. 5
    
6.
Einarsdottir E, Carlsson A, Minde J, Toolanen G, Svensson O, Solders G, et al. A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception. Hum Mol Genet 2004;13:799-805.  Back to cited text no. 6
    
7.
Narayanan V. Oral and maxillofacial manifestations of hereditary sensory neuropathy. Br J Oral Maxillofac Surg 1996;34:446-9.  Back to cited text no. 7
    
8.
Jacob A, Sarada C, Thomas SV. Painless injuries in a child: Hereditary sensory and autonomic neuropathy. Ann Indian Acad Neurol 2006;9:39-41.  Back to cited text no. 8
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9.
Indo Y, Tsuruta M, Hayashida Y, Karim MA, Ohta K, Kawano T, et al. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. Nat Genet 1996;13:485-8.  Back to cited text no. 9
    
10.
de Andrade DC, Baudic S, Attal N, Rodrigues CL, Caramelli P, Lino AM, et al. Beyond neuropathy in hereditary sensory and autonomic neuropathy type V: Cognitive evaluation. Eur J Neurol 2008;15:712-9.  Back to cited text no. 10
    
11.
Prashanth GP, Kamate M. A case of hereditary sensory autonomic neuropathy type IV. Ann Indian Acad Neurol 2012;15:134-6.  Back to cited text no. 11
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12.
Haga N, Kubota M, Miwa Z. Epidemiology of hereditary sensory and autonomic neuropathy type IV and V in Japan. Am J Med Genet A 2013;161A: 871-4.  Back to cited text no. 12
    
13.
Tomioka T, Awaya Y, Nihei K, Sekiyama H, Sawamura S, Hanaoka K. Anesthesia for patients with congenital insensitivity to pain and anhidrosis: A questionnaire study in Japan. Anesth Analg 2002;94:271-4.  Back to cited text no. 13
    
14.
Okuda K, Arai T, Miwa T, Hiroki K. Anaesthetic management of children with congenital insensitivity to pain with anhidrosis. Paediatr Anaesth 2000;10:545-8.  Back to cited text no. 14
    
15.
Mitaka C, Tsunoda Y, Hikawa Y, Sakahira K, Matsumoto I. Anesthetic management of congenital insensitivity to pain with anhydrosis. Anesthesiology 1985;63:328-9.  Back to cited text no. 15
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  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]



 

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