| Literature DB >> 30677142 |
Marcella Zollino1,2, Christiane Zweier3, Ingrid D Van Balkom4,5, David A Sweetser6, Joseph Alaimo7, Emilia K Bijlsma8, Jannine Cody9, Sarah H Elsea7, Irina Giurgea10, Marina Macchiaiolo11, Robert Smigiel12, Ronald L Thibert13, Ingrid Benoist14, Jill Clayton-Smith15, Channa F De Winter16, Stijn Deckers17, Anusha Gandhi7, Sylvia Huisman18, Dagmar Kempink19, Frea Kruisinga18, Vittoria Lamacchia20, Giuseppe Marangi1,2, Leonie Menke18, Paul Mulder4,5, Ann Nordgren21, Alessandra Renieri20, Sue Routledge22, Carol J Saunders23, Agnieszka Stembalska24, Hans Van Balkom25, Sandra Whalen10, Raoul C Hennekam18.
Abstract
Pitt-Hopkins syndrome (PTHS) is a neurodevelopmental disorder characterized by intellectual disability, specific facial features, and marked autonomic nervous system dysfunction, especially with disturbances of regulating respiration and intestinal mobility. It is caused by variants in the transcription factor TCF4. Heterogeneity in the clinical and molecular diagnostic criteria and care practices has prompted a group of international experts to establish guidelines for diagnostics and care. For issues, for which there was limited information available in international literature, we collaborated with national support groups and the participants of a syndrome specific international conference to obtain further information. Here, we discuss the resultant consensus, including the clinical definition of PTHS and a molecular diagnostic pathway. Recommendations for managing particular health problems such as dysregulated respiration are provided. We emphasize the need for integration of care for physical and behavioral issues. The recommendations as presented here will need to be evaluated for improvements to allow for continued optimization of diagnostics and care.Entities:
Keywords: Pitt-Hopkins syndrome; TCF4; autonomic dysfunction; diagnostic criteria; guidelines; molecular diagnostic pathway; syndromic behavior
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Year: 2019 PMID: 30677142 DOI: 10.1111/cge.13506
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438