Abstract
We report on a young female patient diagnosed with Marfan syndrome upon admission to the psychiatric hospital for a first psychosis. Mutation analysis of FBN1 identified a de novo nonsense mutation (p.Glu178X). This finding implies co-occurrence of schizophrenia and Marfan syndrome, an observation that has been reported several times in the past. Although, this co-occurrence can be coincidental, several arguments provide strong evidence that Marfan syndrome and schizophrenia might share common etiological pathways. This observation can be important in light of both the etiology of schizophrenia and the diagnosis of Marfan syndrome.
| Original language | English |
|---|---|
| Pages (from-to) | 252-5 |
| Number of pages | 4 |
| Journal | European Journal of Medical Genetics |
| Volume | 55 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Apr 2012 |
| Externally published | Yes |
Keywords
- Codon, Nonsense
- DNA Mutational Analysis
- Female
- Fibrillin-1
- Fibrillins
- Genotype
- Humans
- Marfan Syndrome/complications
- Microfilament Proteins/genetics
- Pedigree
- Phenotype
- Schizophrenia/complications
- Young Adult
- Adipokines
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