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Report Overview

Familial adenomatous polyposis (FAP) is a rare inherited disorder with near-certain colorectal cancer risk by middle age, making early genetic testing, regular surveillance, and timely prophylactic surgery essential. The familial adenomatous polyposis epidemiology forecast by Expert Market Research indicates that the rising emphasis on preventing colorectal cancer will likely boost the diagnosis rate of familial adenomatous polyposis in the coming years.

2025

Base Year

2019-2025

Historical Period

2026-2035

Forecast Period

Familial Adenomatous Polyposis (FAP) – Number Of Cases By Year

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Familial Adenomatous Polyposis (FAP) Epidemiology Forecast Report Coverage

Expert Market Research's “Familial Adenomatous Polyposis (FAP) Epidemiology Forecast Report 2026-2035” offers comprehensive information on the prevalence and demographics of familial adenomatous polyposis (FAP). It projects the future incidence and prevalence rates of familial adenomatous polyposis (FAP) cases across various populations. The study covers age, gender, and type as major determinants of the familial adenomatous polyposis (FAP) population. The report highlights patterns in the prevalence of familial adenomatous polyposis (FAP) over time and projects future trends based on multiple variables.

The report provides a comprehensive overview of the disease, as well as historical and projected data on familial adenomatous polyposis (FAP) epidemiology in the 8 major markets.

Regions Covered

  • The United States
  • Germany
  • France
  • Italy
  • Spain
  • The United Kingdom
  • Japan
  • India

Familial Adenomatous Polyposis (FAP) Understanding: Disease Overview

Familial adenomatous polyposis (FAP) is an autosomal dominant hereditary syndrome caused by germline mutations in the APC gene, leading to the formation of hundreds to thousands of adenomatous colorectal polyps. Without prophylactic surgery, nearly all patients develop colorectal cancer by middle age. The condition may also involve duodenal adenomas and extracolonic tumors such as desmoid or thyroid neoplasms. Two primary variants exist, namely, classic FAP and attenuated FAP (AFAP), which differ in polyp number, age of onset, and cancer risk.

Familial Adenomatous Polyposis (FAP) Epidemiology Perspective

The familial adenomatous polyposis (FAP) epidemiology division offers information on the patient pool from history to the present, as well as the projected trend for each of the 8 major markets. Expert Market Research provides both current and predicted trends for the familial adenomatous polyposis (FAP) epidemiology scenario by examining a wide range of studies. Additionally, the report covers the diagnosed patient pool for familial adenomatous polyposis (FAP) and their trends. The familial adenomatous polyposis (FAP) detailed epidemiology segmentation is broken down into specific categories, such as total prevalent cases in males and females, and total diagnosed cases across different age groups and patient pools.

  • Familial adenomatous polyposis has an estimated prevalence of approximately 1 in 8,000 to 1 in 18,000 individuals, accounting for about 0.5% of all colorectal cancer cases globally.
  • Polyps typically develop by adolescence, with the average age of onset being around 16 years.
  • Without intervention, the risk of developing colorectal cancer is nearly 100% by the 5th decade of life, with the average age of diagnosis being 40 years.
  • Early detection through genetic testing and regular screenings, such as colonoscopy, is crucial. Colectomy is often recommended once polyps emerge to prevent cancer development.

Familial Adenomatous Polyposis (FAP) – Number Of Cases By Country

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Country-wise Familial Adenomatous Polyposis (FAP) Epidemiology Segment

The familial adenomatous polyposis (FAP) epidemiology data and findings for the United States, Germany, Spain, Italy, France, the United Kingdom, Japan, and India are also provided in the epidemiology section.

Familial adenomatous polyposis (FAP) is a rare inherited disorder with an estimated prevalence ranging from 1 in 5,000 to 1 in 18,000 live births in the U.S. It accounts for less than 1% of all colorectal cancer cases in the country. The condition is characterized by the development of numerous adenomatous polyps in the colon and rectum, typically manifesting during adolescence. If left untreated, individuals with FAP have a nearly 100% risk of developing colorectal cancer by the age of 40. Early diagnosis through genetic testing and regular screening, such as colonoscopy, is crucial for effective management. Prophylactic colectomy is often recommended upon detection of polyps to mitigate cancer risk.

Familial Adenomatous Polyposis (FAP): Treatment Overview

The management aims to prevent colorectal cancer through early detection and surgical intervention. Prophylactic colectomy, either total proctocolectomy with ileal pouch-anal anastomosis or colectomy with ileorectal anastomosis, is the definitive treatment. Nonsteroidal anti-inflammatory drugs (NSAIDs) like celecoxib or sulindac may reduce polyp burden but do not eliminate cancer risk. Lifelong endoscopic surveillance is essential for the remaining rectal and upper gastrointestinal mucosa. Genetic counselling and screening of at-risk family members enable early diagnosis and timely intervention to improve long-term survival outcomes.

Key Questions Answered

  • What are the key findings of familial adenomatous polyposis (FAP) epidemiology in the 8 major markets?
  • What will be the total number of patients with familial adenomatous polyposis (FAP) across the 8 major markets during the forecast period?
  • What was the country-wise familial adenomatous polyposis (FAP) epidemiology scenario in the 8 major markets in the historical period?
  • Which country will have the highest number of cases of familial adenomatous polyposis (FAP) during the forecast period of 2026-2035?
  • Which key factors would influence the shift in the patient population of familial adenomatous polyposis (FAP) during the forecast period of 2026-2035?
  • What are the currently available treatments for familial adenomatous polyposis (FAP)?
  • What are the disease risks, signs, symptoms, and unmet needs of familial adenomatous polyposis (FAP)?

Scope of the Familial Adenomatous Polyposis (FAP) Epidemiology Report

  • The report covers a detailed analysis of signs and symptoms, causes, risk factors, pathophysiology, diagnosis, treatment options, and classification/types of familial adenomatous polyposis (FAP) based on several factors.
  • Familial Adenomatous Polyposis (FAP) Epidemiology Forecast Report covers data for the eight major markets (the US, France, Germany, Italy, Spain, the UK, Japan, and India).
  • The familial adenomatous polyposis (FAP) report helps to identify the patient population, and the unmet needs are highlighted along with an assessment of the disease's risk and burden.

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Please note that the figures mentioned in the description serve as estimates and may vary from the actual figures presented in the final report.

Report Features 

Details 

Base Year 

2025

Historical Period

2019-2025

Forecast Period

2026-2035

Epidemiology Statistics Provided

  • Diagnosed Prevalent Cases
  • Type-Specific Cases
  • Gender-Specific Cases
  • Age-Specific Cases

Segmentation Provided

  • Epidemiology by Age Group
  • Epidemiology by Gender
  • Epidemiology by Type of Disease
  • Epidemiology by Region

Geographies Covered 

  • United States
  • Germany
  • Italy
  • France
  • Spain
  • United Kingdom
  • Japan
  • India

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