Johanson–Blizzard's Syndrome with a Novel UBR1 Mutation

Damla Demir; Yasemin Kendir Demirkol; Nelgin Gerenli; Ezgi Aktaş Karabay

doi:10.1055/s-0040-1716331

Journal of Pediatric Genetics, Inhaltsverzeichnis

J Pediatr Genet 2022; 11(02): 147-150
DOI: 10.1055/s-0040-1716331

Case Report

Johanson–Blizzard's Syndrome with a Novel UBR1 Mutation

Damla Demir

¹Department of Dermatology, Ümraniye Training and Research Hospital, University of Health Science, Istanbul, Turkey

,

Yasemin Kendir Demirkol

²Department of Pediatrics Genetics, Ümraniye Training and Research Hospital, University of Health Science, Istanbul, Turkey

,

Nelgin Gerenli

³Department of Pediatrics Gastroenterology, Ümraniye Training and Research Hospital, University of Health Science, Istanbul, Turkey

,

Ezgi Aktaş Karabay

⁴Department of Dermatology, Faculty of Medicine, Bahçeşehir University, Istanbul, Turkey

› Institutsangaben

Abstract

Johanson–Blizzard syndrome (JBS) is a rare autosomal recessive genetic disorder, characterized by exocrine pancreatic insufficiency, a distinct abnormal facial appearance and varying degrees of growth retardation. Ubiquitin protein ligase E3 component n-recognin 1 (UBR1) gene mutations are responsible for the syndrome. Here, we describe a 2-month-old female infant, who presented with oily diarrhea, facial dysmorphia, scalp defect, hearing defects, and growth impairment. Molecular genetic testing revealed a novel frameshift mutation in UBR1, c.4027_4028 del (p.Leu1343Valfs*7), which was not previously described in JBS in the literature.

Keywords

aplasia cutis - facial dysmorphia - Johanson–Blizzard's syndrome - novel variants - pancreatic insufficiency - UBR1 gene

Volltext

Referenzen

References
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