World Library  
Flag as Inappropriate
Email this Article

Congenital insensitivity to pain with anhidrosis

Article Id: WHEBN0001124428
Reproduction Date:

Title: Congenital insensitivity to pain with anhidrosis  
Author: World Heritage Encyclopedia
Language: English
Subject: Hypoalgesia, Hereditary sensory and autonomic neuropathy, Familial dysautonomia, Congenital insensitivity to pain, Pain
Collection: Autosomal Recessive Disorders, Neurocutaneous Conditions, Peripheral Nervous System Disorders, Rare Diseases
Publisher: World Heritage Encyclopedia
Publication
Date:
 

Congenital insensitivity to pain with anhidrosis

Congenital insensitivity to pain with anhidrosis
Classification and external resources
OMIM 256800
DiseasesDB 32097
MeSH D009477

Congenital insensitivity to pain with anhidrosis (CIPA), also called hereditary sensory and autonomic neuropathy type IV—is an extremely rare inherited disorder of the nervous system which prevents the sensation of pain, heat, cold, or any real nerve-related sensations (including feeling the need to urinate); however, patients can still feel pressure. CIPA is the fourth type of hereditary sensory and autonomic neuropathy (HSAN), known as HSAN IV. (It is also referred to as HSAN Type IV). A person with CIPA cannot feel pain or differentiate even extreme temperatures. "Anhidrosis" means the body does not sweat, and "congenital" indicates that the condition is present from birth.

Contents

  • Clinical description 1
  • Differential diagnosis 2
  • Cause 3
  • In the media 4
  • References 5
  • External links 6

Clinical description

Charcot joints are demonstrated in this boy with HSAN IV or congenital insensitivity to pain with anhidrosis (CIPA). The right knee and right ankle (on the left of the picture) are enlarged and distorted. The skin over the medial aspect of the ankle is darkened with a draining wound secondary to superimposed osteomyelitis. There are other areas of trauma and ulcers including a site on the right heel.

People with this disorder are very likely to injure themselves in ways that would normally be prevented by feeling pain. For example, a patient could burn themselves severely and not even notice. The main features of the disorder are lack of pain sensation, painless injuries of the arms, legs and oral structures, hyperthermia during hot weather because of inability to sweat, syndromic intellectual disability as a result of hyperthermia, infection and scarring of the tongue, lips and gums, chronic infections of bones and joints, bone fractures, multiple scars, osteomyelitis and joint deformities, which may lead to amputation. Other common problems are eye related, such as infection due to the sufferers rubbing them too hard, too frequently or scratching them during sleep. In addition, patients typically lack unmyelinated and small myelinated nerve fibers in the dorsal root ganglion. Both are responsible for transmitting pain signals. In addition, patients' sweat glands are normal in both structure and function, though they lack innervations by small diameter neurons.[1]

Differential diagnosis

Congenital insensitivity to pain with anhidrosis may be misdiagnosed for leprosy, based on similar symptoms of severe injuries to the hands and feet.

Cause

CIPA is caused by a genetic mutation which prevents the formation of nerve cells which are responsible for transmitting signals of pain, heat, and cold to the brain. The disorder is autosomal recessive. It does not appear to have any particular ethnic distribution, though it is more prevalent in cultures in which intermarriage is an accepted practice.[2] Overheating kills more than half of all children with CIPA before age 3.

The genetic mutation is in the gene encoding the neurotrophic tyrosine kinase receptor (NTRK1 gene).[3] NTRK1 is a receptor for nerve growth factor (NGF). This protein induces outgrowth of axons and dendrites and promotes the survival of embryonic sensory and sympathetic neurons. The mutation in NTRK1 does not allow NGF to bind properly, causing defects in the development and function of nociceptive reception.[4]

In the media

The manga and anime series Loveless features 4 characters, the Zero, with this condition. Notably they were genetically engineered to possess it as their creator believed being unable to feel pain would make them better warriors.

In the third season of the TV series Mika Boorem) suffers from this condition. In the third season of the TV series Grey's Anatomy in the episode "Sometimes a Fantasy", Abigail Breslin's character, Megan Clover, is diagnosed with this condition.

In the original visual novel, as well as the anime adaptation of DRAMAtical Murder, it is stated that of the main characters, Noiz, suffers from this condition which led to his parents abandoning him, and he is known to frequently cut and injure his hands without noticing.

CIPA is examined in an episode of Mystery Diagnosis entitled The Boy Who Never Cried, featuring a child suffering from the disorder. The child's condition first emerges after the tip of their tongue ulcerates and is accidentally bitten off by the repeated action of it moving against the child's growing incisor teeth.

In the first season of the TV series The Blacklist in the episode "The Courier (No. 85)" (5th episode), the Courier, a criminal transporter, is diagnosed with congenital anhidrosis.

References

  1. ^ Abdel-Hafez, Hisham; Sarah Mohamed Awad (June 2007). "Congenital Insensitivity to Pain with Anhidrosis (CIPA)". Egyptian Dermatology Online Journal 3 (1). Retrieved 7 December 2011. 
  2. ^ Mardy, Sek; Yuichi Miura; Fumio Endo; Ichiro Matsuda; Yasuhiro Indo (2001). "Congenital Insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor". Human Molecular Genetics 10 (3): 179–188.  
  3. ^ Shatzky S, Moses S, Levy J; et al. (June 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". Am. J. Med. Genet. 92 (5): 353–60.  
  4. ^ Indo, Yasuhiro. "Mutations in the TRKA/NGF Receptor Gene in Patients with Congenital Insensitivity to Pain with Anhidrosis" (PDF). Kumamoto University. Retrieved 7 December 2011. 

External links

  • The Facts of Painless People The website of two adults on separate sides of the world who were born with CIPA.
  • Help Roberto The website of young boy with CIPA. Features Roberto's specific case, information about CIPA, and links to videos on CNN and the Discovery Channel. (Site has ended, link from Archive.org)
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and USA.gov, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for USA.gov and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
 
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
 
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.
 



Copyright © World Library Foundation. All rights reserved. eBooks from Hawaii eBook Library are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.