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September 25, 2026BMC PediatricsOpen Access

Intrafamilial phenotypic variability in pediatric Wolfram syndrome associated with a homozygous WFS1 p.(Tyr669Ter) variant: a Palestinian family case series

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Authors

DMDima MalhisLMLana MalhisMSMuna Sharaf

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Malhis et al. (2026) studied this question.

synapsesocial.com/papers/6ab60edd406bf401c1467703https://doi.org/10.1186/s12887-026-07756-9
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  1. 160 Wolfram syndrome with variable presentation: case series2024 · 1 citations
  2. 2 gene mutation associated with pediatric diabetes mellitus and congenital deafness: A case report.2025
  3. 3Expanding the phenotype of Wolfram syndrome: adult presentation with a novel <i>WFS1</i> variant2026
  4. 4Wolfram syndrome: Identification of a phenotypic and genotypic variant from Jordan2002 · 38 citations
  5. 5Late Recognition of Wolfram Syndrome Type 1 in Adulthood: Multisystemic Presentation with a Founder WFS1 Variant &amp;ndash; A case report2026