{
  "abstract": "A boy is born at full term with no complications during pregnancy or delivery. At a routine two week visit with his GP, he is jaundiced with yellow stools but is gaining weight. The GP attributes jaundice to breast milk and recommends to continue breastfeeding. At four weeks, his mother notes occasional pale-yellow coloured stools on several days. The GP reviews photographs of the stool, and the stools appear pigmented in some photos and lacking pigment in others. He advises the mother to continue observing. Jaundice persists at two months, and when the child attends for his first set of immunisations, the mother reports that all stools have become chalk coloured.",
  "authors": [
    {
      "affiliations": [
        "Division of Gastroenterology, Hepatology, Nutrition, Stanford University, Stanford, CA, USA"
      ],
      "name": "Tebyan Rabbani"
    },
    {
      "affiliations": [
        "Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA",
        "Patient author"
      ],
      "name": "Ahmad Anouti"
    },
    {
      "affiliations": [
        "Department of Pediatrics, Unidad Médica de Alta Especialidad, Mérida, Yucatán, México"
      ],
      "name": "Ana Gabriela Ayala German"
    },
    {
      "affiliations": [
        "Division of Neonatal-Perinatal Medicine, University of Michigan, Ann Arbor, MI, USA"
      ],
      "name": "Jacqueline Meadow"
    },
    {
      "affiliations": [
        "Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, University of Texas Southwestern, Children’s Medical Center, Dallas, TX, USA"
      ],
      "name": "Sindhu Pandurangi"
    }
  ],
  "title": "Easily missed?: Early recognition of biliary atresia",
  "uid": "df1a9c69-18cd-5b66-bea4-007218e6a8d8"
}