Homozygous SQSTM1 nonsense variant identified in a patient with brainstem involvement

Kilic M. A., Kipoglu O., Coskun O., Karacabey B. N., Yesilyurt A., Yildiz E., ...Daha Fazla

BRAIN & DEVELOPMENT, cilt.43, sa.10, ss.1039-1043, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Sayı: 10
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.braindev.2021.06.001
  • Dergi Adı: BRAIN & DEVELOPMENT
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, EMBASE, MEDLINE, Psycinfo
  • Sayfa Sayıları: ss.1039-1043
  • Anahtar Kelimeler: Ataxia, SQSTM1, P62, Myoclonus, Brainstem, Eye movement abnormalities, MUTATION
  • İstanbul Üniversitesi Adresli: Evet

Özet

In recent years, with advances in molecular genetics, many new mutations with various ataxic syndromes have been identified. Recently, homozygous sequestosome 1 (SQSTM1) gene variant with a progressive childhood-onset cerebellar ataxia, dystonia and gaze palsy was described. Here we describe a patient with progressive cerebellar ataxia and gaze palsy, as well as myoclonus, cognitive impairment and growth retardation with a homozygous SQSTM1 variant NM 003900.5:c.55G > T (p.Glu19*). Our case had brainstem lesions on brain magnetic resonance imaging that have not been previously reported. This novel finding expands the SQSTM1 gene-associated neuroradiologic spectrum. Homozygous SQSTM1 variant should be considered in the differential diagnosis in patients presenting with cerebellar findings, gaze palsy, and cognitive impairment to facilitate early diagnosis and genetic counseling. (C) 2021 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.