Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases

Roberto Colombo, Roeltje R. Maas, Katarzyna Iwanicka-Pronicka, Sema Kalkan Ucar, Bader Alhaddad, Moeenaldeen Alsayed, Mohammed A. Al-Owain, Hamad I. Al-Zaidan, Shanti Balasubramaniam, Ivo Barić, Dalal K. Bubshait, Alberto Burlina, John Christodoulou, Wendy K. Chung, Niklas Darin, Peter Freisinger, Maria Teresa Garcia Silva, Stephanie Grunewald, Tobias B. Haack, Peter M. Van HasseltOmar Hikmat, Friederike Hörster, Pirjo Isohanni, Khushnooda Ramzan, Reka Kovacs-Nagy, Zita Krumina, Elena Martin-Hernandez, Johannes A. Mayr, Patricia Mcclean, Linda De Meirleir, Karin Naess, Lock H. Ngu, Magdalena Pajdowska, Shamima Rahman, Gillian Riordan, Lisa Riley, Benjamin Roeben, Frank Rutsch, Rene Santer, Manuel Schiff, Martine Seders, Silvia Sequeira, Wolfgang Sperl, Christian Staufner, Matthis Synofzik, Robert W. Taylor, Joanna Trubicka, Konstantinos Tsiakas, Ozlem Unal, Evangeline Wassmer, Yehani Wedatilake, Toni Wolff, Holger Prokisch, Eva Morava, Ewa Pronicka, Ron A. Wevers, Arjan P. De Brouwer, Saskia B. Wortmann

Risultato della ricerca: Contributo in rivistaArticolo in rivista

14 Citazioni (Scopus)

Abstract

Objective: 3-Methylglutaconic aciduria, dystonia–deafness, hepatopathy, encephalopathy, Leigh-like syndrome (MEGDHEL) syndrome is caused by biallelic variants in SERAC1. Methods: This multicenter study addressed the course of disease for each organ system. Metabolic, neuroradiological, and genetic findings are reported. Results: Sixty-seven individuals (39 previously unreported) from 59 families were included (age range = 5 days–33.4 years, median age = 9 years). A total of 41 different SERAC1 variants were identified, including 20 that have not been reported before. With the exception of 2 families with a milder phenotype, all affected individuals showed a strikingly homogeneous phenotype and time course. Severe, reversible neonatal liver dysfunction and hypoglycemia were seen in >40% of all cases. Starting at a median age of 6 months, muscular hypotonia (91%) was seen, followed by progressive spasticity (82%, median onset = 15 months) and dystonia (82%, 18 months). The majority of affected individuals never learned to walk (68%). Seventy-nine percent suffered hearing loss, 58% never learned to speak, and nearly all had significant intellectual disability (88%). Magnetic resonance imaging features were accordingly homogenous, with bilateral basal ganglia involvement (98%); the characteristic “putaminal eye” was seen in 53%. The urinary marker 3-methylglutaconic aciduria was present in virtually all patients (98%). Supportive treatment focused on spasticity and drooling, and was effective in the individuals treated; hearing aids or cochlear implants did not improve communication skills. Interpretation: MEGDHEL syndrome is a progressive deafness–dystonia syndrome with frequent and reversible neonatal liver involvement and a strikingly homogenous course of disease. Ann Neurol 2017;82:1004–1015.
Lingua originaleEnglish
pagine (da-a)1004-1015
Numero di pagine12
RivistaAnnals of Neurology
Volume82
DOI
Stato di pubblicazionePubblicato - 2017

Keywords

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Carboxylic Ester Hydrolases
  • Child
  • Child, Preschool
  • Cohort Studies
  • Deaf-Blind Disorders
  • Disease Progression
  • Dystonia
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Intellectual Disability
  • Male
  • Mutation
  • Neurology
  • Neurology (clinical)
  • Optic Atrophy
  • Young Adult

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