# Constitutional indocyanine green excretion defect in a Chinese patient without underlying liver disease: case report and mechanistic insights

## TL;DR

A Chinese patient without liver disease showed a rare indocyanine green excretion defect, offering new insights into its cause.

## Contribution

First documented Chinese case of CIED without liver disease and no known transporter gene mutations.

## Key findings

- No pathogenic variants found in known ICG transporter genes in the patient.
- Suggests novel pathogenesis for CIED independent of established transporter deficiencies.

## Abstract

Constitutional indocyanine green excretion defect (CIED) is a rare disorder characterized by markedly delayed plasma indocyanine green disappearance (ICG-R15 > 50%) despite normal results from conventional liver function tests. We present case a case involving 60-year-old woman diagnosed with CIED, which represents the first documented case in a Chinese patient without any underlying liver disease. This case expands the recognized geographic and epidemiologic spectrum of CIED. Whole-exome sequencing revealed no deletions or pathogenic variants in genes encoding established ICG transporters [SLCO1B1 (OATP1B1), SLCO1B3 (OATP1B3), SLC10A1 (NTCP), and ABCC2 (MRP2)], excluding conventional mechanistic explanations. Our integrated clinical and molecular characterization offers novel insights into this rare disorder. These findings suggest a novel pathogenesis independent of known transporter deficiencies, highlighting the need for further research and underscoring the importance of integrating multidimensional clinical data for accurate interpretation of ICG test results.