{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T08:49:24Z","timestamp":1788425364611,"version":"build-2803163510"},"reference-count":17,"publisher":"American Academy of Pediatrics (AAP)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2000,1,1]]},"abstract":"<jats:p>In the 1920s, a little girl 3 years of age was brought from China to the United States by her American mother. Although the child was beautiful, her mind was not developing. The grief-stricken mother had consulted doctors in China, but they could neither diagnose the problem nor provide treatment. Morning and night the same questions occupied her mind: \u201cWhat is the matter with my little girl? What is causing it? Is there any doctor, anywhere, who can cure her?\u201d<\/jats:p><jats:p>In the United States, she also went from doctors to psychologists to clinics looking for someone who could help. Finally, she went to the Mayo Clinic in Rochester, Minnesota. When she had answered all of the doctor's questions, and all the tests were finished, they still could not tell her what was wrong. There was nothing they could do. The disease from which the little girl suffered was unknown at that time.<\/jats:p><jats:p>The mother was Pearl Buck. In her book, The Child Who Never Grew,1 she described her first infant: \u201cI remember when she was only 3 months old she lay in her basket on the sun deck of a ship. I had taken her there for the morning air. The people who promenaded on deck often stopped to look at her, and my pride grew as they spoke of her unusual beauty and of the intelligent look of her deep, blue eyes. I do not know at what moment the growth of her intelligence stopped, nor to this day why it did.\u201d<\/jats:p><jats:p>This is a classical description of the disease, phenylketonuria (PKU). A perfect infant seems to develop normally for several months, then the development slows and at some point seems to stop. \u201cLook at Mommy\u2014look at Daddy!\u201d the parents say as they try to coax the treasured smiles. Instead, the child drifts into a dream world and into irreversible mental retardation.<\/jats:p><jats:p>All Pearl Buck's devotion and determination was of no avail in finding the cause of her child's retardation. It was to be another mother with the same commitment to her beautiful but retarded children, who approximately 10 years later followed the same path until she found a special doctor who unlocked the secret of the fate of these children.<\/jats:p><jats:p>When 1 of the authors (W.R.C.) visited Miss Buck at her Pennsylvania home in 1960, she talked about how her daughter, Carol, then a grown person, had recently been diagnosed as having PKU, as a result of screening tests at the New Jersey Vineland Training School for the Mentally Retarded. During my visit and without disclosing the reason, Pearl Buck was invited to sniff a vial of phenylacetate crystals (the odor of stale urine samples from PKU patients). Immediately she recalled that Carol, as a child, had the same unusual odor. She was relieved that the prophesy of the last words in her book had come true: \u201cWhat has been, need not forever continue to be so. It is too late for some of our children, but if their plight can make people realize how unnecessary much of the tragedy is, their lives, thwarted as they are, will not have been meaningless.\u201d<\/jats:p><jats:p>These could be the words of Borgny Egeland, the mother of the children through whom the mystery of PKU was brought to light. Or they could express the conviction of the physician and biochemist, Asbjo\u0308rn Fo\u0308lling, who believed that \u201cwhat was not known could be known.\u201d Through the discovery of PKU in these children, hope has been given to thousands of other children and to their grateful parents (Fig 1).<\/jats:p>","DOI":"10.1542\/peds.105.1.89","type":"journal-article","created":{"date-parts":[[2004,8,13]],"date-time":"2004-08-13T23:50:41Z","timestamp":1092441041000},"page":"89-103","source":"Crossref","is-referenced-by-count":92,"title":["The Discovery of Phenylketonuria: The Story of a Young Couple, Two Retarded Children, and a Scientist"],"prefix":"10.1542","volume":"105","author":[{"given":"Siegried A.","family":"Centerwall","sequence":"first","affiliation":[{"name":"From the Child Health and Disability Prevention, California State Department of Health Services, Sacramento, California; and the"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Willard R.","family":"Centerwall","sequence":"additional","affiliation":[{"name":"Departments of Pediatrics and Genetics and Medical Genetic Services, Universities of California at Davis and of Loma Linda, California."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"417","published-online":{"date-parts":[[2000,1,1]]},"reference":[{"key":"2021121010271440200_B1"},{"key":"2021121010271440200_B2","doi-asserted-by":"crossref","first-page":"651","DOI":"10.1016\/S0021-9258(17)30882-7","article-title":"Studies on phenylpyruvic oligophrenia: position of metabolic error.","volume":"169","author":"Jervis","year":"1947","journal-title":"J Biol Chem"},{"key":"2021121010271440200_B3","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1093\/jhmas\/XVI.3.292","article-title":"Phenylketonuria (Fo\u0308lling's Disease): the story of its discovery.","volume":"16","author":"Centerwall","year":"1961","journal-title":"J Hist Med Allied 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