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Autor
Afenjar, Alexandra 1 Alembik, Yves 1 Alessandri, Jean-Luc 1 Arpin, Stéphanie 1 Barcia, Giulia 1 Bendová, Šárka 1 Bruel, Ange-Line 1 Burger, Pauline 1 Charles, Perrine 1 Chatron, Nicolas 1 Chaumette, Boris 1 Chopra, Maya 1 Conrad, Solène 1 Cospain, Auriane 1 Coubes, Christine 1 Coursimault, Juliette 1 Daire, Valérie Cormier 1 Delahaye-Duriez, Andrée 1 Doco, Martine 1 Dufour, William 1
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APHP La Pitié Salpétrière Paris France 1 APHP Trousseau Paris France 1 CH Saint Brieuc Service de Génétique Saint B... 1 CHU La Réunion Service de génétique Saint De... 1 Center for Rare Psychiatric Disorders GHU Pa... 1 Centre Hospitalier Universitaire de Reims Pô... 1 Centre de Génétique et Centre de référence m... 1 Child Neurology and Psychiatry Unit Azienda ... 1 Department of Biology and Medical Genetics C... 1 Department of Genetics and Reference Center ... 1 Department of Medical Genetics University Ho... 1 Department of Neurology Rosamund Stone Zande... 1 Department of Pathology and Laboratory Medic... 1 Department of Psychiatry McGill University M... 1 Département de Génétique Centre de Référence... 1 Département de Génétique Centre de référence... 1 Département de Génétique Paris Centre de Réf... 1 Genetic Department CEA Paris Saclay NeuroSpi... 1 Genetic Department CHU Lille Clinique de Gén... 1 Genetic Department CHU Nantes Service de Gén... 1
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NLK
Directory of Open Access Journals
od 2013
Free Medical Journals
od 2013
PubMed Central
od 2013
Europe PubMed Central
od 2013
ProQuest Central
od 2013-05-01
Open Access Digital Library
od 2013-01-01
Open Access Digital Library
od 2013-01-01
Wiley-Blackwell Open Access Titles
od 2013
PubMed
38284452
DOI
10.1002/mgg3.2363
Knihovny.cz E-zdroje
INTRODUCTION AND METHODS: We report two series of individuals with DDX3X variations, one (48 individuals) from physicians and one (44 individuals) from caregivers. RESULTS: These two series include several symptoms in common, with fairly similar distribution, which suggests that caregivers' data are close to physicians' data. For example, both series identified early childhood symptoms that were not previously described: feeding difficulties, mean walking age, and age at first words. DISCUSSION: Each of the two datasets provides complementary knowledge. We confirmed that symptoms are similar to those in the literature and provides more details on feeding difficulties. Caregivers considered that the symptom attention-deficit/hyperactivity disorder were most worrisome. Both series also reported sleep disturbance. Recently, anxiety has been reported in individuals with DDX3X variants. We strongly suggest that attention-deficit/hyperactivity disorder, anxiety, and sleep disorders need to be treated.
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