Altay, Derya2024-07-112024-07-112019-05-010019-5456https://doi.org/10.1007/s12098-018-2833-7https://hdl.handle.net/11452/43207ObjectiveCholestatic jaundice in early infancy is a complex diagnostic challenge. Cholestasis caused by endocrine disease is rare and poorly recognized. The aim of this paper is to report patients with liver dysfunctions resulting from hypopituitarism.MethodsSix patients with liver dysfunction diagnosed as hypopituitarism were studied and followed up atUludag University Faculty of Medicine.ResultsThe median age of the patients at first presentation was 2.5 mo. Three patients were diagnosed with congenital hypopituitarism at the first visit, and the other three were diagnosed during follow-up. Serum aminotransferase levels were very high in two patients and only moderately elevated in the others. Combined adrenal, thyroid, and growth hormone deficiencies were diagnosed in two patients, while remaining 4 patients had various combinations of adrenal, thyroid, and growth hormone deficiencies. Liver function abnormalities resolved between 10 d and 2 mo follow-up after hormone replacement therapy.ConclusionsAbnormal liver biochemical test results due to hormonal deficiencies in infants should be considered in the differential diagnosis by pediatricians. Hormone replacement therapy is the basis of treatment.eninfo:eu-repo/semantics/closedAccessNeonatal cholestasisHypoglycemiaJaundiceInfantsCholestasisHyperbilirubinemiaHypopituitarismScience & technologyLife sciences & biomedicinePediatricsArticle00046759810000641241686510.1007/s12098-018-2833-7