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Vici Syndrome Associated with Sensorineural Hearing Loss and Evidence of Neuromuscular Involvement on Muscle Biopsy by Verity McClelland; Thomas Cullup; Istvan Bodi; Deborah Ruddy; Anna Buj‐Bello; Valerie Biancalana; J. Boehm; Marc Bitoun; Owen Miller; Wajanat Jan; Esse Menson; Luis Amaya; John Trounce; Jocelyn Laporte; Shehla Mohammed; Caroline Sewry; Julian Raiman; Heinz Jungbluth is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Vici Syndrome Associated with Sensorineural Hearing Loss and Evidence of Neuromuscular Involvement on Muscle Biopsy about?

## Abstract Vici syndrome is a rare, genetically unresolved congenital multisystem disorder comprising agenesis of the corpus callosum, cataracts, immunodeficiency, cardiomyopathy, and hypopigmentation. An associated neuromuscular phenotype has not previously been described in detail. We report on an infant with clinical features suggestive of Vici syndrome and additional sensorineural hearing loss. Muscle biopsy revealed several changes including markedly increased variability in fiber size, increased internal nuclei, and abnormalities on Gomori trichrome and oxidative stains, raising a wide differential diagnosis including neurogenic atrophy, centronuclear myopathy (CNM) or a metabolic (mitochondrial) cytopathy. Respiratory chain enzyme studies, however, were normal and sequencing of common CNM‐associated genes did not reveal any mutations. This case expands the clinical spectrum of Vici syndrome and indicates that muscle biopsy ought to be considered in infants presenting with suggestive clinical features. In addition, we suggest that Vici syndrome is considered in the differential diagnosis of infants presenting with congenital callosal agenesis and that additional investigatio

Who reads Vici Syndrome Associated with Sensorineural Hearing Loss and Evidence of Neuromuscular Involvement on Muscle Biopsy?

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Verity McClelland; Thomas Cullup; Istvan Bodi; Deborah Ruddy; Anna Buj‐Bello; Valerie Biancalana; J. Boehm; Marc Bitoun; Owen Miller; Wajanat Jan; Esse Menson; Luis Amaya; John Trounce; Jocelyn Laporte; Shehla Mohammed; Caroline Sewry; Julian Raiman; Heinz Jungbluth
Publisher
John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 1552-4825)
Published
2010
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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