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the claim

Congenital insensitivity to pain was documented and is extremely rare

the verdict
SUPPORTED
the evidence backs this
Recorded sources
11 sources for · 0 against

Counts group repeated records of the same source within each side. They do not measure evidence strength or source independence.

Congenital insensitivity to pain has been well-documented in medical literature and is universally recognized as an extremely rare condition.

The analysis

The retrieved papers consistently document congenital insensitivity to pain (often referred to as CIPA or HSAN) and repeatedly emphasize its extreme rarity through various case reports and literature reviews. The claim is fully supported by the evidence.

Evidence for · 11
Recorded source metadata

L. M. Pérez-López, M. Cabrera-González, D. Gutiérrez-de la Iglesia, S. Ricart, G. Knörr-Giménez. Update Review and Clinical Presentation in Congenital Insensitivity to Pain and Anhidrosis. 2015. https://doi.org/10.1155/2015/589852

States that congenital insensitivity to pain and anhidrosis (CIPA) is an extremely rare syndrome.

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More for · 10
Recorded source metadata

A. López-Cortés, A. Zambrano, P. Guevara-Ramírez, B. A. Echeverría, Santiago Guerrero, E. Cabascango, A. Pérez-Villa, I. Armendáriz-Castillo, J. García-Cárdenas, V. Yumiceba, G. Pérez-M, P. Leone, C. Paz-y-Miño. Clinical, genomics and networking analyses of a high-altitude native American Ecuadorian patient with congenital insensitivity to pain with anhidrosis: a case report. 2020. https://doi.org/10.1186/s12920-020-00764-3

Notes that CIPA is an extremely rare autosomal recessive disorder characterized by insensitivity to pain.

Recorded source metadata

Liena Gasina, Nityanand Jain, Arturs Viksne, D. Ozols, Mohit Kakar, Uldis Bergmanis. Recurrent Osteomyelitis in a Paediatric Patient with a Novel NTRK1 Mutation: A Case Report on Congenital Insensitivity to Pain with Anhidrosis. 2025. https://doi.org/10.3390/children12030344

Identifies CIPA as an exceedingly rare genetic disorder characterized by the inability to perceive pain.

Recorded source metadata

H. Hamdani, N. Mtalai, Sara Ennaki, G. Daghouj, L. E. Maaloum, B. Allali, A. Kettani, L. E. Maaloum. Congenital Insensitivity TO Pain: A Case Report. 2023. https://doi.org/10.24018/ejmed.2023.5.4.1782

Describes congenital insensitivity to pain as a rare genetic disorder and references historical documentation beginning in the 1930s.

Recorded source metadata

N. Al-Hroub, A. Alsalahat, M. Taamreh, Fawzy M. Abunejma, Osama N. Dukmak. Congenital Insensitivity to Pain: A Case Study of a Rare Genetic Disorder. 2024. https://doi.org/10.7759/cureus.69414

Classifies congenital insensitivity to pain as an exceedingly rare autosomal recessive condition.

Recorded source metadata

Malek N. Itmaiza, Adriana J. Skafi, A. Adawi, Peter R Bael, Nouraldin M M Ibaidi. First instance of pain in congenital pain insensitivity with anhidrosis.. 2025. https://doi.org/10.1016/j.clineuro.2025.108775

Describes a case of a patient known to have congenital insensitivity to pain and notes the syndrome's rarity.

Recorded source metadata

Xiong Q, Huang L, Hu Y, Fu W. Case Report: Arthroscopic synovectomy and loose body removal for charcot knee in an adolescent with congenital insensitivity to pain with anhidrosis.. 2026. https://doi.org/10.3389/fsurg.2026.1767073

Notes that Charcot neuroarthropathy in adolescents with congenital insensitivity to pain with anhidrosis is exceptionally rare.

Recorded source metadata

Temur KT. Uncovering oral and maxillofacial clues in congenital insensitivity to pain with anhidrosis: what can sibling cases teach us?. 2025. https://doi.org/10.1186/s12903-025-07202-9

Describes CIPA as an extremely congenital disorder characterized by severe clinical manifestations including pain insensitivity.

Recorded source metadata

Karabinos A, Tomkova E, Sprincova A, Tothova K, Repiska V, Jesenak M, Krizan P. A Novel Inflammatory Autoimmune-Like <i>NTRK1</i>-Associated Phenotype in an Adult Man.. 2025. https://doi.org/10.1159/000549961

Notes that CIPA is a rare autosomal recessive disorder characterized by congenital analgesia.

Recorded source metadata

Abdel-Bari ABAT, Fawzy M, Saad KA, Alhadainy HA. Multidisciplinary Approach for Dental Management of Congenital Insensitivity to Pain with Anhidrosis: Clinical Case Report with 12-Month Follow-Up.. 2026. https://doi.org/10.3390/dj14010068

States that congenital insensitivity to pain and anhidrosis is a rare autosomal recessive disorder.

Recorded source metadata

Lala S, Almustafa A. Oral Rehabilitation in Patient With Hereditary Sensory and Autonomic Neuropathy (HSAN) Type V: Clinical Report.. 2025. https://doi.org/10.1155/crid/6868923

The paper trail · every fact has a biography
first checked02 Aug 2026
judged → SUPPORTED · 8302 Aug 2026
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