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Aniridia with PAX6 mutations and narcolepsy.
Berntsson, Shala Ghaderi; Kristoffersson, Anna; Daniilidou, Makrina; Dahl, Niklas; Ekström, Curt; Semnic, Robert; Markström, Agneta; Niemelä, Valter; Partinen, Markku; Hallböök, Finn; Landtblom, Anne-Marie.
Affiliation
  • Berntsson SG; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Kristoffersson A; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Daniilidou M; Department of Clinical and Experimental Medicine, Neurology, Medical Faculty, University of Linköping, Linköping, Sweden.
  • Dahl N; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Ekström C; Science for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
  • Semnic R; Department of Neuroscience, Ophthalmology, Uppsala University, Uppsala, Sweden.
  • Markström A; Section of Neuroradiology, Department of Radiology, Uppsala University, Uppsala, Sweden.
  • Niemelä V; Department of Medical Sciences, Respiratory, Allergy, and Sleep Research, Uppsala University, Uppsala, Sweden.
  • Partinen M; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Hallböök F; Vitalmed Research Center, Helsinki Sleep Clinic, Helsinki, Finland.
  • Landtblom AM; Department of Clinical Neurosciences, University of Helsinki, Helsinki, Finland.
J Sleep Res ; 29(6): e12982, 2020 12.
Article in En | MEDLINE | ID: mdl-31943460
PAX6 gene mutations cause a variety of eye and central nervous system (CNS) abnormalities. Aniridia is often accompanied by CNS abnormalities such as pineal gland atrophy or hypoplasia, leading to disturbed circadian rhythm and sleep disorders. Less is known on the coincidence of narcolepsy in this patient group. We aimed to find out whether the circadian rhythm or sleep-wake structure was affected in patients with aniridia. Four members of a family segregating with congenital aniridia in two generations were included in the study. The patients were subjected to genetic testing for a PAX6 mutation, multiple sleep latency test, whole-brain magnetic resonance imaging (MRI), hypocretin-1 in cerebrospinal fluid, and Human Leukocyte Antigen DQ beta1*06:02. All four members were heterozygous for the pathogenic c.959-1G>A mutation in the PAX6 gene. Sleep disturbance was observed in all family members. The index patient was diagnosed with narcolepsy. MRI showed a hypoplastic pineal gland in all members. We describe the first case of a patient with PAX6 haploinsufficiency, aniridia and pineal gland hypoplasia diagnosed with narcolepsy type-1, suggesting a complex sleep disorder pathogenesis.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aniridia / PAX6 Transcription Factor / Narcolepsy Limits: Adult / Female / Humans / Middle aged Language: En Journal: J Sleep Res Journal subject: PSICOFISIOLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aniridia / PAX6 Transcription Factor / Narcolepsy Limits: Adult / Female / Humans / Middle aged Language: En Journal: J Sleep Res Journal subject: PSICOFISIOLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication: