Diagnosis and management in Pitt-Hopkins syndrome: First international consensus statement.
Pitt-Hopkins syndrome
TCF4
autonomic dysfunction
diagnostic criteria
guidelines
molecular diagnostic pathway
syndromic behavior
Journal
Clinical genetics
ISSN: 1399-0004
Titre abrégé: Clin Genet
Pays: Denmark
ID NLM: 0253664
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
19
11
2018
revised:
20
12
2018
accepted:
09
01
2019
pubmed:
25
1
2019
medline:
19
5
2020
entrez:
25
1
2019
Statut:
ppublish
Résumé
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.
Substances chimiques
Transcription Factor 4
0
Types de publication
Consensus Development Conference
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
462-478Informations de copyright
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.