# Progressive Polycystic Kidney Disease in an Infant Girl With TSC2/PKD1 Contiguous Gene Syndrome

**Authors:** Kazuhiko Hashimoto, Takuya Hayashida, Yoshikazu Otsubo, Yo Niida, Sumito Dateki

PMC · DOI: 10.7759/cureus.67800 · 2024-08-26

## TL;DR

This paper reports a case of a rare genetic syndrome in an infant girl that causes kidney disease and brain abnormalities, highlighting the need for early diagnosis and monitoring.

## Contribution

The study emphasizes the importance of early genetic testing and longitudinal imaging for managing TSC2/PKD1 contiguous gene syndrome in infants.

## Key findings

- The infant girl had TSC2/PKD1 contiguous gene syndrome confirmed by microarray analysis.
- Polycystic kidney lesions enlarged rapidly, leading to early childhood hypertension.
- Longitudinal abdominal imaging is crucial for tracking disease progression in this syndrome.

## Abstract

TSC2/PKD1 contiguous gene syndrome is caused by deletions involving the TSC2 and PKD1 genes that lead to tuberous sclerosis complex and autosomal dominant polycystic kidney disease. It is characterized by early-onset severe cystic kidney disease with progressive enlargement of the kidneys and the cysts. As it can lead to early hypertension and an accelerated decline of kidney function, early genetic testing is needed for early diagnosis of this syndrome, and more frequent imaging-based examinations are necessary to assess disease progression and determine appropriate management. We report the case of an infant girl with TSC2/PKD1 contiguous gene syndrome who presented with epileptic seizures. Brain magnetic resonance imaging (MRI) revealed subependymal nodules and cortical tubers, and abdominal MRI revealed polycystic kidney lesions and enlargement of both kidneys. TSC2/PKD1 contiguous gene syndrome was suspected from her radiological features, and we confirmed the presence of a deletion in the girl’s genome, which included the TSC2 and PKD1 genes, via microarray analysis. Thereafter, we evaluated the change in kidney size via repeated abdominal MRI. The polycystic kidney lesions enlarged, and the patient developed hypertension in early childhood, for which we administered an angiotensin-converting enzyme inhibitor. We emphasize the importance of evaluation with longitudinal abdominal imaging because renal cysts tend to enlarge rapidly and induce hypertension, as demonstrated in our case.

## Linked entities

- **Genes:** TSC2 (TSC complex subunit 2) [NCBI Gene 7249], PKD1 (polycystin 1, transient receptor potential channel interacting) [NCBI Gene 5310]
- **Diseases:** tuberous sclerosis complex (MONDO:0001734), autosomal dominant polycystic kidney disease (MONDO:0004691)

## Full-text entities

- **Genes:** PKD1 (polycystin 1, transient receptor potential channel interacting) [NCBI Gene 5310] {aka PBP, PC1, Pc-1, TRPP1, eliosin}, TSC2 (TSC complex subunit 2) [NCBI Gene 7249] {aka LAM, PPP1R160, TSC4}
- **Diseases:** autosomal dominant polycystic kidney disease (MESH:D016891), cysts (MESH:D003560), Contiguous Gene Syndrome (MESH:D025063), enlargement (MESH:D006332), hypertension (MESH:D006973), kidneys (MESH:D007674), epileptic seizures (MESH:D004827), cystic kidney disease (MESH:D052177), tuberous sclerosis complex (MESH:D014402), Polycystic Kidney Disease (MESH:D007690)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11423392/full.md

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Source: https://tomesphere.com/paper/PMC11423392