Congenital insensitivity to pain with anhidrosis (CIPA) is a rareautosomal recessive disorder of the nervous system which prevents the feeling of pain or temperature and prevents a person from sweating. Cognitive disorders are commonly coincidental. CIPA is the fourth type of hereditary sensory and autonomic neuropathy (HSAN), and is also known as HSAN IV.
Signs and symptoms
Signs of CIPA are present from infancy. Infants may present with seizures related to an abnormally high body temperature. Since people with this condition are unable to sweat, they are unable to properly regulate their body temperature.[1] Those affected are unable to feel pain and temperature.[2][3]
The absence of pain experienced by people with CIPA puts them at high risk for accidental self-injury. Corneal ulceration occurs due to lack of protective impulses.[4] Joint and bone problems are common due to repeated injuries, and wounds heal poorly.[5]
Delayed developmental milestones in early years may be observed.[6]
Patients often have severe learning difficulties, irritability, hyperactivity, self-injurious behaviour, and cognitive impairment,[6] but patients with normal intelligence have also been reported.[6]
Cause
CIPA is caused by a genetic mutation that prevents the formation of nerve cells responsible for transmitting signals of pain, heat, and cold in the brain.
The disorder is inherited in an autosomal recessive fashion.[6]
CIPA is caused by a mutation in NTRK1,[6] a gene encoding the neurotrophic tyrosine kinase receptor.[7] 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.[3]
Mitochondrial abnormalities in muscle cells have been found in people with CIPA. Skin biopsies show a lack of innervation of the eccrine glands[4] and nerve biopsies show a lack of small myelinated and unmyelinated fibers.[4][8][3]
Diagnosis
Diagnosis is made based on clinical criteria, supported by nerve biopsy findings of reduced unmyelinated and small myelinated fibres, and can be confirmed with genetic testing.[1][2]
Differential diagnosis
The absence of or significantly reduced sweating in CIPA patients can be used for a differential diagnosis.[6]
Treatment
There is no treatment for CIPA. Attention to injuries to prevent infection and worsening is necessary.[1]
Anaesthetic management
Some patients with CIPA have been operated on without anesthesia,[9] but the patient's anxiety might still need to be alleviated in these cases.[9]
Patients might have tactile hyperesthesia, in which case anesthesia is necessary.[9]
^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. doi:10.1002/1096-8628(20000619)92:5<353::AID-AJMG12>3.0.CO;2-C. PMID10861667.
^Volpe's Neurology of the Newborn (6 ed.). Elsevier. 2018. pp. 887–921.
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