# The long way to diagnosis: attention disorder, alcohol addiction or congenital disorder of glycosylation? A case report

**Authors:** Timo Jendrik Faustmann, Lukas Hensel, Armin Bahic, Yoshinao Wada, Marianne Grüneberg, Thorsten Marquardt, Daniel Kamp, Leonhard Schilbach

PMC · DOI: 10.1186/s12888-025-06862-9 · 2025-04-29

## TL;DR

A young woman with ADHD-like symptoms was found to have a rare metabolic disorder instead of alcohol addiction.

## Contribution

Highlights the importance of considering metabolic disorders like CDG in patients presenting with ADHD symptoms and high CDT levels.

## Key findings

- A patient's high CDT levels were caused by a transferrin mutation, not alcohol addiction.
- Psychiatric symptoms can be linked to underlying metabolic disorders such as CDG.
- Differential diagnosis in ADHD should include ruling out SUD and metabolic conditions.

## Abstract

Attention deficit hyperactivity disorder (ADHD) is a relatively common disorder in clinical psychiatry. Patients often suffer from symptoms long before the diagnosis due to an overlap with other psychiatric differential diagnosis. Importantly, alcohol addiction and other illicit drug dependence and withdrawal symptoms mimicking ADHD symptoms should be ruled out. Here we present a rare case of a young female patient with symptoms of ADHD and an extremely high carbohydrate-deficient transferrin (CDT) of 19,6% (< 1,3%) indicating the presence of a congenital disorder of glycosylation (CDG). A thorough diagnostic workup excluded alcohol addiction as a cause of the constantly high CDT levels. The CDT test was positive due a transferrin mutation affecting the glycosylation site. Nevertheless, psychiatric symptoms can be due to metabolic disorders which should be considered. Further, substance-use disorders (SUD) are a critical and potentially complicated differential diagnosis concerning diagnostic procedures and treatment in ADHD.

The online version contains supplementary material available at 10.1186/s12888-025-06862-9.

## Linked entities

- **Proteins:** Tsf2 (transferrin 2)
- **Diseases:** Attention deficit hyperactivity disorder (MONDO:0007743), alcohol addiction (MONDO:0002046), congenital disorder of glycosylation (MONDO:0015286)

## Full-text entities

- **Genes:** TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}
- **Diseases:** psychiatric (MESH:D001523), metabolic disorders (MESH:D008659), alcohol addiction (MESH:D000437), CDG (MESH:D018981), withdrawal (MESH:D013375), carbohydrate (MESH:C562602), SUD (MESH:D019966), ADHD (MESH:D001289), deficient transferrin (MESH:C537248)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12042650/full.md

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Source: https://tomesphere.com/paper/PMC12042650