Two Cases With Neonatal Cholestasis and Renal Disorders Due to DCDC2 Mutation
- 1 May 2022
- journal article
- research article
- Published by Baskent University in Experimental and Clinical Transplantation
- Vol. 20 (Suppl 3) , 115-117
Abstract
Ciliopathies are a heterogeneous group of diseases that are observed after deterioration of the ciliary structures on the cell surface that facilitate communication with the environment. Both liver and kidney involvement are frequently observed in this disease. Recently, a doublecortin domain containing protein 2 (DCDC2) mutation in a ciliopathy disease group was identified. Here, we present 2 patients with this mutation and with neonatal cholestasis and renal involvement.Keywords
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