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Congenital Insensitivity To Pain (CIP): Causes, Symptoms, Complications, Diagnosis And Treatment
Congenital insensitivity to pain or (CIP) is a rare genetic disorder of the nervous system in which a person is unable to perceive any kind of physical pain. It is an autosomal recessive disorder, meaning an inherited disorder caused when the two copies of abnormal gene get transferred to the child and cause the trait for this problem to develop. The disorder is usually present at the birth of an individual [1] .
People with CIP are unable to feel pain in any body parts due to lack of senses. For example, they cannot sense whether a certain object is hot or cold and are unable to detect any wound in their body parts which often cause them multiple injuries, infection, broken bones and other serious health problems due to lack of senses. Due to the repeated injuries, their life expectancy is also decreased.
CIP is also considered a type of peripheral neuropathy, a disorder of the peripheral nervous system which is responsible for the exchange of signals (smell, touch and pain) between the central nervous system and other body parts or vice versa [2] .
CIP is known by several names. The other names of CIP include the following:
- Congenital sensory, with anhidrosis [2]
- Neuropathy
- Hereditary sensory and autonomic neuropathy 4
- Familial dysautonomia, type II
Causes Of Congenital Insensitivity To Pain
A gene named SCN9A is responsible to provide instructions to the body to make a part of the alpha subunit (protein) called Nav1.7 which is responsible for the transmission of electric signals (pain, heat and cold) to the brain and spinal cord.
The mutation in the gene SCN9A causes nonfunctional alpha subunits leading to the death of the neurons. This results in the loss of sensory neurons, causing an obstruction in the passage of pain signals from the affected body parts to the brain, hence leading to CIP [3] .
Symptoms Of Congenital Insensitivity To Pain
Symptoms of people with CIP vary from individual to individual. Common symptoms of the condition are as follows:
- Seizures due to hyperthermia, as people with CIP, are often unable to sweat (anhidrosis) [4]
- Unable to feel pain [1]
- Unable to feel the temperature
- Loss of smell, anosmia [5]
- Loss of bladder control [6]
- Severe spasticity of the lower limbs [7]
Complications Of Congenital Insensitivity To Pain
Complications of CIP include the following:
- Severe burn or injuries [1]
- Painless fractures [8]
- Infection due to insensitivity to wounds [9]
- Corneal abrasions due to decreased tear production [10]
- Anhidrosis, loss of very less production of sweat [11]
- Urinary incontinence [1]
- Chronic anaemia [12]
Diagnosis Of Congenital Insensitivity To Pain
Diagnosing CIP can be problematic for healthcare experts. It is carried out by the following processes:
- Medical history: To get a detailed view of the symptoms of a patient with CIP and rule out other similar conditions.
- Genetic Testing Registry (GTR): A comprehensive genetic test information about the patient who has voluntarily submitted it for testing [13] .
Treatment Of Congenital Insensitivity To Pain
There is still no cure available for treating CIP. However, the condition can be managed by controlling the complications of the disorder. As it develops from birth, parents and caretakers of a child with CIP should be careful and provide immediate medical attention when any of the complications occur. For serious bone problems in children, surgeries are advised while for infection, wounds, and loss of tear production, related drugs are prescribed [1] .
- [1] Peddareddygari, L. R., Oberoi, K., & Grewal, R. P. (2014). Congenital insensitivity to pain: a case report and review of the literature. Case reports in neurological medicine, 2014, 141953. doi:10.1155/2014/141953
- [2] Labib, S., Adnane Berdai, M., Abourazzak, S., Hida, M., & Harandou, M. (2011). Congenital insensitivity to pain with anhydrosis: report of a family case. The Pan African medical journal, 9, 33.
- [3] Peddareddygari, L. R., Oberoi, K., & Grewal, R. P. (2014). Congenital insensitivity to pain: a case report and review of the literature. Case reports in neurological medicine, 2014, 141953. doi:10.1155/2014/141953
- [4] Sasnur, A. H., Sasnur, P. A., & Ghaus-Ul, R. S. (2011). Congenital insensitivity to pain and anhidrosis. Indian journal of orthopaedics, 45(3), 269–271. doi:10.4103/0019-5413.80047
- [5] Zhang, S., Malik Sharif, S., Chen, Y. C., Valente, E. M., Ahmed, M., Sheridan, E., … Woods, G. (2016). Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain. Journal of medical genetics, 53(8), 533–535. doi:10.1136/jmedgenet-2015-103646
- [6] Indo Y. Congenital Insensitivity to Pain with Anhidrosis. 2008 Aug 5 [Updated 2014 Apr 17]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
- [7] Borsook D. (2012). Neurological diseases and pain. Brain : a journal of neurology, 135(Pt 2), 320–344. doi:10.1093/brain/awr271
- [8] Phatarakijnirund, V., Mumm, S., McAlister, W. H., Novack, D. V., Wenkert, D., Clements, K. L., & Whyte, M. P. (2016). Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9. Bone, 84, 289–298. doi:10.1016/j.bone.2015.11.022
- [9] Daneshjou, K., Jafarieh, H., & Raaeskarami, S. R. (2012). Congenital Insensitivity to Pain and Anhydrosis (CIPA) Syndrome; A Report of 4 Cases. Iranian journal of pediatrics, 22(3), 412–416.
- [10] Amano, S., Fukuoka, S., Usui, T., Honda, N., Ideta, R., Ochiai, M., ... & Awaya, Y. (2006). Ocular manifestations of congenital insensitivity to pain with anhidrosis. American journal of ophthalmology, 141(3), 472-477.
- [11] Soussou, R., Cheung, W. S., & Campbell, K. M. (2019). Congenital Insensitivity to Pain with Anhidrosis: A Case with Self-Inflicted Oral Ulcerations. Journal of Dentistry for Children, 86(2), 109-112.
- [12] Shatzky, S., Moses, S., Levy, J., Pinsk, V., Hershkovitz, E., Herzog, L., ... & Parvari, R. (2000). Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli‐Bedouins: Genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies. American journal of medical genetics, 92(5), 353-360.
- [13] Rubinstein, W. S., Maglott, D. R., Lee, J. M., Kattman, B. L., Malheiro, A. J., Ovetsky, M., … Ostell, J. M. (2013). The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency. Nucleic acids research, 41(Database issue), D925–D935. doi:10.1093/nar/gks1173
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