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Summer's Complaint

My family's courageous, century-long struggle with a rare genetic cancer syndrome

Laura Kieger

ca. 6,49
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Ratgeber / Gesundheit


Familial Adenomatous Polyposis, or FAP, accounts for roughly 1 percent of hereditary colorectal cancer and carries an extremely high lifetime risk of colon cancer and elevated risks for other exceedingly rare cancers. It is an autosomal dominant condition caused by germline mutations in the adenomatous polyposis coli (APC) gene. By the age of fifty, nearly 99 percent of untreated FAP patients will have developed cancer.

This is the dark shadow that has lingered over one family since at least 1911, when a matriarch was first seen at the Mayo Clinic in Rochester, Minnesota for symptoms that would become commonplace in her descendants. Three of her five children died in their thirties with what they’d come to call “summer’s complaint” (a variant of the general diagnosis “summer complaint” often given to infants and children facing severe intestinal/gastric maladies). Her granddaughter, genetically programmed by a defect on her 5th chromosome also developed colon cancer, which would ultimately take her life. Five of her eight great-grandchildren carried the APC mutation, three of whom were diagnosed with gastrointestinal cancers at an average age of forty-nine. Two of her great-great-grandchildren who carried the gene mutation died of associated brain and liver cancers, one at thirty-one, the other just shy of his third birthday.

This is that family's sometimes tragic story. As told by a daughter, aunt, and sister who was spared the mutation but has been surrounded by its relentless destruction her entire life, Summer’s Complaint is at once a testament to the courage of those one family has lost and a journey toward understanding hereditary predispositions to disease and how best to combat them.

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APC, FAP, DNA, colon cancer, genetics, familial adenomatous polyposis, inherited disorders, Lynch Syndrome