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<p><i>MYCBP2</i>-associated neurodevelopmental disorder is an autosomal dominant genetic disorder, previously described with de novo variants. We present the case of a two-generation review of a proband with a maternally inherited heterozygous pathogenic variant in <i>MYCBP2</i>, c.4409dup (p.Leu1470Phefs*7). Neuropsychology assessment indicated developmental delays with proband’s scores falling well below age-level expectations, while proband’s mother demonstrated generally intact cognition with evidence of subtle executive inefficiency. Assessment of parental genotype and phenotype can help to anticipate child’s developmental trajectory, especially in genetic disorders associated with highly variable expressivity. However information gaps on familial impact of inherited neurodevelopmental disorders across generations remain.</p>

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First report of an inherited MYCBP2 neurodevelopmental disorder: review of proband and parent presentation

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月16日

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  • Alice Pham,
  • Jennifer Harmon,
  • Lia K. Thibodaux,
  • Laura A. Flashman,
  • Michelle Curtin

摘要

MYCBP2-associated neurodevelopmental disorder is an autosomal dominant genetic disorder, previously described with de novo variants. We present the case of a two-generation review of a proband with a maternally inherited heterozygous pathogenic variant in MYCBP2, c.4409dup (p.Leu1470Phefs*7). Neuropsychology assessment indicated developmental delays with proband’s scores falling well below age-level expectations, while proband’s mother demonstrated generally intact cognition with evidence of subtle executive inefficiency. Assessment of parental genotype and phenotype can help to anticipate child’s developmental trajectory, especially in genetic disorders associated with highly variable expressivity. However information gaps on familial impact of inherited neurodevelopmental disorders across generations remain.