Two novel cases expanding the phenotype of SETD2‐related overgrowth syndrome |
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| Authors: | Maartje C van Rij Iris H I M Hollink Paulien Anna Terhal Sarina G Kant Claudia Ruivenkamp Arie van Haeringen J Anneke Kievit Martine J van Belzen |
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| Institution: | 1. Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands;2. Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands;3. Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands |
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| Abstract: | The SETD2‐related overgrowth syndrome is also called “Luscan‐Lumish syndrome” (OMIM 616831) with the clinical characteristics of intellectual disability, speech delay, macrocephaly, facial dysmorphism, and autism spectrum disorders. We report on two novel patients a 4.5‐year‐old boy and a 23‐year‐old female adolescent with a speech and language developmental delay, autism spectrum disorder and macrocephaly, who were both diagnosed with SETD2‐related overgrowth syndrome due to de novo frameshift mutations in the SETD2 gene. Features not previously described which were present in either one of our patients were nasal polyps, a large tongue with creases, a high pain threshold, constipation, and undescended testicles. These features may be related to the syndrome and may need special attention in future patients. Additionally, prevention of obesity should be an important point of attention for patients diagnosed with a SETD2‐related overgrowth syndrome. |
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| Keywords: | autism Luscan‐Lumish syndrome obesity OMIM 616831 overgrowth SETD2 Sotos‐like syndrome |
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