| Literature DB >> 22378662 |
Ilenia Maini1, Gaetano Cantalupo, Emanuela Claudia Turco, Fernando De Paolis, Cinzia Magnani, Liborio Parrino, Mario Giovanni Terzano, Francesco Pisani.
Abstract
Pitt-Hopkins syndrome is a rare genetic form of severe psychomotor delay, caused by mutations in transcription cell factor-4 gene and characterized by distinctive dysmorphic features and abnormal breathing pattern. The current report describes the polygraphic features of the syndrome's typical breathing pattern in a patient both in wakefulness and in sleep. The control of these breathing alterations is important to prevent the neurological sequelae linked to chronic cerebral hypoxemia in early ages. No data are available on effective treatment options for breathing abnormalities of Pitt-Hopkins syndrome. The authors polygraphically documented a reduction of apneic and hypopneic phenomena, with a significant improvement in saturation values, after the introduction of sodium valproate.Entities:
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Year: 2012 PMID: 22378662 DOI: 10.1177/0883073811435917
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987