Article
Phenotypic and Genetic Insights Into CNOT3-Related Intellectual Developmental Disorder of Speech Delay, Autism, and Dysmorphic Faces (IDDSADF) From the First Two Japanese Cases.
American journal of medical genetics. Part A - 1 Oct 2026
Ariyasu Daisuke, Kosaki Rika, Cho Hideo, Nakashima Moeko, Tsuchihashi Takatoshi, Kosaki Kenjiro, Yamazawa Kazuki
Abstract excerpt
Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Faces (IDDSADF) is a rare neurodevelopmental disorder caused by heterozygous variants in CNOT3. Although several cohorts have been documented worldwide, no Japanese patients have been reported to date. Here, we present the first two Japanese cases of IDDSADF, an 8-year-old girl and a 19-year-old boy, both presenting with developmental...
Read the complete abstract on PubMedTopics
- Humans
- Child
- Male
- Female
- Language Development Disorders
- Phenotype
