Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome

Am J Med Genet A. 2021 Dec;185(12):3576-3583. doi: 10.1002/ajmg.a.61854. Epub 2020 Sep 21.

Abstract

It has been estimated that 10-15% of people with Robinow syndrome (RS) show delayed development, but no studies have formally assessed developmental domains. The objective of this study is to provide the first description of cognitive, adaptive, and psychological functioning in RS. Thirteen participants (10 males) aged 4-51 years were seen for neuropsychological screening. Eight had autosomal-dominant RS (DVL1, n = 5; WNT5A, n = 3), four had autosomal-recessive RS (NXN, n = 2; ROR2, n = 2), and one had a mutation on an RS candidate gene (GPC4). Participants completed measures of intellectual, fine-motor, adaptive, executive, and psychological functioning. Findings indicated generally average intellectual functioning and low-average visuomotor skills. Adaptive functioning was average in autosomal-recessive RS (RRS) but low average in autosomal-dominant RS (DRS). Parent-report indicated executive dysfunction and attention problems in 4/8 children, 3/4 of whom had a DVL1 variant; adult self-report did not indicate similar difficulties. Learning disabilities were also reported in 4/8 individuals with DRS, 3/4 of whom had a DVL1 variant. Peer problems were reported for a majority of participants, many of whom also reported emotional concerns. Altogether, the findings indicate average neurocognitive functioning in RRS. In contrast, DRS, especially DVL1 pathogenic alleles, may confer specific risk for neurodevelopmental disability.

Keywords: Robinow syndrome; adaptive; cognitive; psychological; social.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Alleles
  • Child
  • Child, Preschool
  • Craniofacial Abnormalities / epidemiology
  • Craniofacial Abnormalities / genetics*
  • Craniofacial Abnormalities / physiopathology
  • Developmental Disabilities / epidemiology
  • Developmental Disabilities / genetics*
  • Developmental Disabilities / physiopathology
  • Dishevelled Proteins / genetics*
  • Dwarfism / epidemiology
  • Dwarfism / genetics*
  • Dwarfism / physiopathology
  • Genetic Predisposition to Disease
  • Humans
  • Learning Disabilities / genetics
  • Learning Disabilities / physiopathology
  • Limb Deformities, Congenital / epidemiology
  • Limb Deformities, Congenital / genetics*
  • Limb Deformities, Congenital / physiopathology
  • Male
  • Middle Aged
  • Neurocognitive Disorders / epidemiology
  • Neurocognitive Disorders / genetics*
  • Neurocognitive Disorders / physiopathology
  • Phenotype
  • Psychosocial Functioning
  • Urogenital Abnormalities / epidemiology
  • Urogenital Abnormalities / genetics*
  • Urogenital Abnormalities / physiopathology
  • Wnt-5a Protein / genetics*
  • Young Adult

Substances

  • DVL1 protein, human
  • Dishevelled Proteins
  • WNT5A protein, human
  • Wnt-5a Protein

Supplementary concepts

  • Robinow Syndrome