Literature DB >> 29610177

NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central Apnea.

Jamie Campbell1, David R FitzPatrick2, Tara Azam3, Neil A Gibson4, Laura Somerville5, Shelagh K Joss6, Don S Urquhart7.   

Abstract

The sodium leak channel nonselective protein (NALCN) is a regulator of the pacemaker neurons that are responsible for rhythmic behavior (including respiration), maintaining the resting membrane potential, and are required for action potential production. NALCN-null mice show early death associated with disrupted respiratory rhythms, characterized by frequent and profound apneas. We report 3 children (2 siblings) with compound heterozygous mutations in NALCN associated with developmental impairment, hypotonia, and central sleep-disordered breathing causing apneas. Supplemental oxygen normalized the respiratory rhythm. NALCN mutations have been previously reported to cause severe hypotonia, speech impairment, and cognitive delay as well as infantile neuroaxonal dystrophy and facial dysmorphism. Nonsynonymous changes in the 2 affected extracellular loops may be responsible for the deleterious effect on the stability of the respiratory rhythm. Although oxygen is known to be a stabilizer of respiratory rhythm in central apnea in children, its role in NALCN dysfunction requires further investigation.
Copyright © 2018 by the American Academy of Pediatrics.

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Year:  2018        PMID: 29610177     DOI: 10.1542/peds.2017-0026

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  8 in total

1.  Familial Sleep Disorders in Unknown Genetic Syndrome.

Authors:  Mara Lelii; Elena Baggi; Laura Senatore; Maria Francesca Bedeschi; Robertino Dilena; Maria Iascone; Silvana Gangi; Paola Marchisio; Maria Francesca Patria
Journal:  J Pediatr Genet       Date:  2019-10-21

Review 2.  Na+ leak-current channel (NALCN) at the junction of motor and neuropsychiatric symptoms in Parkinson's disease.

Authors:  Merve Kasap; Donard S Dwyer
Journal:  J Neural Transm (Vienna)       Date:  2021-05-07       Impact factor: 3.575

3.  Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).

Authors:  Nuria C Bramswig; Aida M Bertoli-Avella; Beate Albrecht; Aida I Al Aqeel; Amal Alhashem; Nouriya Al-Sannaa; Maissa Bah; Katharina Bröhl; Christel Depienne; Nathalie Dorison; Diane Doummar; Nadja Ehmke; Hasnaa M Elbendary; Svetlana Gorokhova; Delphine Héron; Denise Horn; Kiely James; Boris Keren; Alma Kuechler; Samira Ismail; Mahmoud Y Issa; Isabelle Marey; Michèle Mayer; Jennifer McEvoy-Venneri; Andre Megarbane; Cyril Mignot; Sarar Mohamed; Caroline Nava; Nicole Philip; Cecile Ravix; Arndt Rolfs; Abdelrahim Abdrabou Sadek; Lara Segebrecht; Valentina Stanley; Camille Trautman; Stephanie Valence; Laurent Villard; Thomas Wieland; Hartmut Engels; Tim M Strom; Maha S Zaki; Joseph G Gleeson; Hermann-Josef Lüdecke; Peter Bauer; Dagmar Wieczorek
Journal:  Hum Genet       Date:  2018-08-23       Impact factor: 4.132

4.  Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex.

Authors:  Jinhong Wie; Apoorva Bharthur; Morgan Wolfgang; Vinodh Narayanan; Keri Ramsey; Kimberly Aranda; Qi Zhang; Yandong Zhou; Dejian Ren
Journal:  Nat Commun       Date:  2020-07-03       Impact factor: 14.919

Review 5.  Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.

Authors:  Giacomo Garone; Alessandro Capuano; Lorena Travaglini; Federica Graziola; Fabrizia Stregapede; Ginevra Zanni; Federico Vigevano; Enrico Bertini; Francesco Nicita
Journal:  Int J Mol Sci       Date:  2020-05-20       Impact factor: 5.923

6.  A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature.

Authors:  Amir Hossein Karimi; Mohammad Reza Karimi; Poopak Farnia; Farshid Parvini; Majid Foroutan
Journal:  Appl Clin Genet       Date:  2020-08-27

7.  Structure of voltage-modulated sodium-selective NALCN-FAM155A channel complex.

Authors:  Yunlu Kang; Jing-Xiang Wu; Lei Chen
Journal:  Nat Commun       Date:  2020-12-03       Impact factor: 14.919

8.  Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apnea.

Authors:  Janina Sörmann; Marcus Schewe; Peter Proks; Thibault Jouen-Tachoire; Shanlin Rao; Elena B Riel; Katherine E Agre; Amber Begtrup; John Dean; Maria Descartes; Jan Fischer; Alice Gardham; Carrie Lahner; Paul R Mark; Srikanth Muppidi; Pavel N Pichurin; Joseph Porrmann; Jens Schallner; Kirstin Smith; Volker Straub; Pradeep Vasudevan; Rebecca Willaert; Elisabeth P Carpenter; Karin E J Rödström; Michael G Hahn; Thomas Müller; Thomas Baukrowitz; Matthew E Hurles; Caroline F Wright; Stephen J Tucker
Journal:  Nat Genet       Date:  2022-10-04       Impact factor: 41.307

  8 in total

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