Bilirubin disorders

Abnormal liver function tests and improved survival in a child with splice mutation TARP syndrome
Michael Lane, Nicholas M Allen, Johannes Letshwiti

BMJ Case Reports CP Mar 2023, 16 (3) e253035; DOI: 10.1136/bcr-2022-253035
Novel mutation in the HSD3B7 gene causes bile acid synthetic disorder and presents as recurrent liver failure in early childhood
Yaja Jebaying, Karunesh Kumar, Smita Malhotra, Anupam Sibal

BMJ Case Reports CP Feb 2023, 16 (2) e245852; DOI: 10.1136/bcr-2021-245852
Cystic biliary atresia in a neonate with antenatally detected abdominal cyst
Dafalla Rahamtalla, Yusriya Al Rawahi, Zabah Muhammad Jawa, Yasser Wali

BMJ Case Reports CP Feb 2022, 15 (2) e246081; DOI: 10.1136/bcr-2021-246081
Novel manifestations of Farber disease mimicking neuronopathic Gaucher disease
Shweta Mhatre, Mamta Muranjan, Sunil Karande, Harish Balaji

BMJ Case Reports CP May 2021, 14 (5) e240742; DOI: 10.1136/bcr-2020-240742
High-dose methotrexate-induced reversible grade 4 hyperbilirubinaemia and transaminitis in an adolescent with Burkitt Leukaemia
Sanjeev Khera, Randhir Ranjan, Sateesh Ramachandran, Ajay Beriwal

BMJ Case Reports CP Jan 2021, 14 (1) e237512; DOI: 10.1136/bcr-2020-237512
Progressive familial intrahepatic cholestasis type 4 in an Indian child: presentation, initial course and novel compound heterozygous mutation
Nida Mirza, Ravi Bharadwaj, Smita Malhotra, Anupam Sibal

BMJ Case Reports CP Jul 2020, 13 (7) e234193; DOI: 10.1136/bcr-2019-234193
Prolonged cholestasis after acute viral hepatitis: successfully treated with oral steroid
Manjesh Jayappa, Prawin Kumar, Jagdish Prasad Goyal

BMJ Case Reports CP May 2020, 13 (5) e234430; DOI: 10.1136/bcr-2020-234430
Comorbidity between progressive familial intrahepatic cholestasis and atopic dermatitis in a 19-month-old child
Ilenia Panasiti, Silvana Briuglia, Stefano Costa, Lucia Caminiti

BMJ Case Reports CP Oct 2019, 12 (10) e230152; DOI: 10.1136/bcr-2019-230152

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Bilirubin disorders